Chinese Japanese Germany Korea
ChemicalBook >> CAS DataBase List >>Erlotinib hydrochloride

Erlotinib hydrochloride

Erlotinib hydrochloride Structure
Erlotinib hydrochloride structure
CAS No.
183319-69-9
Chemical Name:
Erlotinib hydrochloride
Synonyms
ERLOTINIB HCL;Tarceva;ErL;Erlotinib, Hydrochloride Salt;CS-491;OSI 774;RG-1415;CP 358774;NSC718781;RO-0508231
CBNumber:
CB2285915
Molecular Formula:
C22H24ClN3O4
Molecular Weight:
429.9
MDL Number:
MFCD07781272
MOL File:
183319-69-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 12:01:10
Product description Number Pack Size Price
Erlotinib hydrochloride ≥98% (HPLC) SML2156 50 mg $71.5
Erlotinib hydrochloride ≥98% (HPLC) SML2156 100 mg $145
Erlotinib Hydrochloride E1404 1G $29
Erlotinib (hydrochloride) ≥98% 35517 50mg $57
Erlotinib (hydrochloride) ≥98% 35517 100mg $85
More product size
Request For Quotation

Erlotinib hydrochloride Properties

Melting point 223-225°C
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Soluble in DMSO (up to 18 mg/ml with warming).
form Yellow powder.
pka pKa (25°): 5.42
color White or off-white
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
InChI InChI=1S/C22H23N3O4.ClH/c1-4-16-6-5-7-17(12-16)25-22-18-13-20(28-10-8-26-2)21(29-11-9-27-3)14-19(18)23-15-24-22;/h1,5-7,12-15H,8-11H2,2-3H3,(H,23,24,25);1H
InChIKey GTTBEUCJPZQMDZ-UHFFFAOYSA-N
SMILES C12C=C(OCCOC)C(OCCOC)=CC=1N=CN=C2NC1=CC=CC(=C1)C#C.Cl
CAS DataBase Reference 183319-69-9(CAS DataBase Reference)
NCI Dictionary of Cancer Terms CP-358; 774; erlotinib hydrochloride; OSI-774
FDA UNII DA87705X9K
NCI Drug Dictionary erlotinib hydrochloride
UNSPSC Code 41116107
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H413
Precautionary statements  P501-P273
Safety Statements  24/25
WGK Germany  WGK 3
RTECS  VA0971200
HS Code  29335990
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
NFPA 704
0
3 0

Erlotinib hydrochloride price More Price(75)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML2156 Erlotinib hydrochloride ≥98% (HPLC) 183319-69-9 50 mg $71.5 2026-04-30 Buy
Sigma-Aldrich SML2156 Erlotinib hydrochloride ≥98% (HPLC) 183319-69-9 100 mg $145 2026-04-30 Buy
TCI Chemical E1404 Erlotinib Hydrochloride 183319-69-9 1G $29 2026-04-30 Buy
Cayman Chemical 35517 Erlotinib (hydrochloride) ≥98% 183319-69-9 50mg $57 2026-04-30 Buy
Cayman Chemical 35517 Erlotinib (hydrochloride) ≥98% 183319-69-9 100mg $85 2026-04-30 Buy
Product number Packaging Price Buy
SML2156 50 mg $71.5 Buy
SML2156 100 mg $145 Buy
E1404 1G $29 Buy
35517 50mg $57 Buy
35517 100mg $85 Buy

Erlotinib hydrochloride Chemical Properties,Uses,Production

Indications and Usage

Erlotinib hydrochlorate is a small molecule tyrosine kinase inhibitor which acts reversibly on epidermal growth factor receptors, a hydrochloride of erlotinib, a molecular-targeted drug. The US Food and Drug Administration (FDA) has approved erlotinib (Tarceva) combined with gemcitabine as a first-line treatment for locally advanced and metastatic pancreatic cancer.
It is mainly used as a second- or third-line treatment for locally advanced or metstatic non-small cell lung cancer (NSCLC) and as a treatment for pancreatic cancer. It is used as a tyrosine inhibitor for NSCLC treatment.

Mechanisms of Action

The small molecular compound erlotinib is a tyrosine kinase receptor inhibitor which inhibits the proliferation of tumor cells by inhibiting phosphorylation, binding to the intracellular catalytic domain of tyrosine kinase in competition with ATP, thus blocking downstream signal transduction and inhibiting activity of tumor cell ligand dependent HER-1/EGFR.

Clinical Research

Phase I clinical trials showed that the main toxicities and side effects of erlotinib were dose-dependent rashes and diarrhea. Other rare side effects included headaches, nausea, and vomiting. Phase II trials used erlotinib as a second-line anticancer drug, with efficacy matching second-line chemotherapy drug docetaxel. Phase III randomized control trials (BR21) mainly focused on NSCLC patients (locally advanced and distant metastasis) after the failure of first- or second-line chemotherapy. The treatment group, with 488 cases in total, took 150mg of erlotinib daily. The control group (243 cases) took a placebo. The study showed:
Median survival rate: 6.7 months for the treatment group, 4.7 months for the control (P<0.001, hazard ratio HR=0.73)
1 year survival rate: 31.2% for the treatment group, 21.5% for the control
Median time of no progression: 9.9 weeks for the treatment group, 7.9 weeks for the control
Meanwhile, symptomatic improvement in the treatment group was more pronounced.
Based on the results of the BR21 study, several further phase III clinical trials were conducted. The TRIBUTE trial combined erlotinib with chemotherapy. The treatment group used chemotherapy (carboplatin + paclitaxel) + erlotinib, while the control used the same chemotherapy alone, with a total of 1,059 late-stage NSCLC patients. The effectiveness of the treatment group was 21.5%, and the control group 19.3%; median survival times were 10.8 and 10.6 months, respectively, and the times of tumor progression (TTP) were 5.1 and 5.0 months. Meanwhile, TALENT trials, with 1,172 NSCLC patients, also investigated the effects of adding erlotinib to chemotherapy (gemcitabine + cisplatin), and also failed to show that erlotinib significantly increased its effects.

Description

Erlotinib, launched as once daily oral treatment for patients with non-small-cell lung cancer (NSCLC), is an inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase, and it is the second small-molecule drug to be marketed with this mechanism of action. Both erlotinib and its predecessor, gefitinib, are members of the anilinoquinazoline class of tyrosine kinase inhibitors. They compete with the binding of ATP to the intracellular tyrosine kinase domain of EGFR, thereby inhibiting receptor autophosphorylation and blocking downstream signal transduction. Erlotinib is prepared by the condensation of 3-ethynylaniline with 4-chloro-6,7-bis(2-methoxyethoxy)quinazoline, which is a key intermediate obtained in five synthetic steps starting from ethyl 3,4- dihydroxybenzoate. In vitro, Erlotinib inhibits purified human EGFR tyrosine kinase with an IC50 of 2 nM and blocks EGFR autophosphorylation in cellular assays with an IC50 of 20nM. Treatment of human colon cancer cells with erlotinib was associated with growth inhibition, G1 cell cycle arrest, and apoptosis. Oral administration of erlotinib in athymic mice produced potent antitumor effects with an ED50 of 9.2 mg/kg/day for HN5 head and neck xenografts and 14 mg/ kg/day for A431 epidermoid xenografts. The absorption of Erlotinib following oral dosing is approximately 60%. Food greatly enhances the absorption allowing for almost 100% bioavailability of the dose. The time to reach peak plasma levels of the drug is about 4 hours, and the half-life is approximately 36 hours. Steady-state drug levels are reached in 7 to 8 days. Erlotinib has high protein binding (93%) and has an apparent volume of distribution of 232 L. It is metabolized primarily by CYP3A4 and to a lesser extent by CYP1A2 and CYP1A1. The drug is mainly excreted in the feces with less than 9% of the dose found in the urine. Erlotinib is labeled for the treatment of patients with locally advanced or metastatic NSCLC who have failed one or more previous chemotherapy regimens. The recommended dosage is 150 mg daily until disease progression is detected. In a randomized, double blind, placebo-controlled trial involving 731 patients, 150 mg/day oral dose of erlotinib resulted in a median overall survival of 6.7 months compared with 4.7 months in the placebo group (p＜0.001). Progression-free survival was 9.9 weeks and 7.9 weeks in the erlotinib and placebo groups, respectively (p＜0.001). Survival at one year was 31.2% in the erlotinib group versus 21.5% in the placebo group. The use of erlotinib showed greater benefit in patients with EGFR positive tumors and in those who never smoked. The most common adverse events reported in clinical trials were rash (9%) and diarrhea (6%). Elevations in liver function tests were also seen; however, these effects were mainly transient or associated with liver metastases. As previously noted for gefitinib, erlotinib is also shown to lack any clinical benefit in concurrent administration with platinum-based chemotherapy.

Chemical Properties

Off-White Solid

Originator

Pfizer (US)

Uses

Erlotinib hydrochloride (V), a quinazoline derived small molecule inhibitor of epidermal growth factor receptor (EDGFR) tyrosine kinase, was approved in November, 2004, for the treatment of advanced or metastatic non-smallcell lung cancer. It belongs to the same class as gefitinib,another quinazoline approved for treatment of advanced lung cancer, but with improved pharmacokinetic properties. The molecule was originated by Pfizer and development initiated in collaboration with OSI, which assumed full rights to the drug when Pfizer merged with Warner Lambert. Subsequently, Genentech/Roche went into licensing agreement with OSI to develop and market the drug in the US and Worldwide.

Uses

Erlotinib HCl (OSI-744) is an EGFR inhibitor with IC50 of 2 nM, >1000-fold more sensitive for EGFR than human c-Src or v-Abl. Phase 3.

Uses

Selective epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor. Antineoplastic

Definition

ChEBI: A quinazoline hydrochloride compound having a (3-ethynylphenyl)amino group at the 4-position and two 2-methoxyethoxy groups at the 6- and 7-positions.

brand name

Tarceva (OSI).

General Description

Erlotinib is available as 25-, 100-, and 150-mg tablets fororal administration and is used after failure of first-linetherapy in metastatic NSCLC and as first-line therapy incombination with gemcitabine in the treatment of metastaticpancreatic cancer, and in treating malignant gliomas.The structural similarity to gefitnib imparts similar pharmacokineticbehavior with bioavailability of 60% and proteinbinding of 93%. The agent is extensively metabolizedprimarily by CYP3A4. Three major metabolic pathwayshave been identified, involving oxidative-O-demethylationof the side chains followed by further oxidation to give thecarboxlic acids, oxidation of the acetylene functionalityto give a carboxylic acid, and aromatic hydroxylation ofthe phenyl ring para to the electron-donating nitrogen. Themetabolites are primarily eliminated in the feces, and theterminal half-life is 36 hours.The major toxicities seenwith the agent are dose-limiting skin rash and diarrhea.Other common adverse effects include shortness of breath,fatigue, and nausea.

Synthesis

The synthesis of this agent is based on the original patent and is shown in the Scheme. The 3,4-dihydroxy benzoate 31 was reacted with bromoethyl methyl ether in the presence of potassium carbonate and tetrabutyl ammonium iodide to give 32 in 93% yield. Nitration followed by hydrogenation provided 34 in 88% yield, which was then cyclized in formamide with ammonium formate to provide quinazolone 35. Subsequent reaction with oxalyl chloride gave quinazoline chloride 36, which was then reacted with 3-ethynyl aniline (37) in isopropanol in the presence of pyridine to give the desired product erlotinib, which was isolated as the HCl salt (V). An alternate synthesis, that used protected 3-trimethylsilyl ethynyl aniline to couple to the quinazoline chloride 36, has also been published.

Synthesis_183319-69-9

target

HER1/EGFR

storage

Store at -20°C

References

[1] J D MOYER. Induction of apoptosis and cell cycle arrest by CP-358,774, an inhibitor of epidermal growth factor receptor tyrosine kinase.[J]. Cancer research, 1997, 57 21: 4838-4848.
[2] ZHE LI. Erlotinib effectively inhibits JAK2V617F activity and polycythemia vera cell growth.[J]. The Journal of Biological Chemistry, 2007, 282 6: 3428-3432. DOI:10.1074/jbc.c600277200
[3] EDGAR R WOOD. A unique structure for epidermal growth factor receptor bound to GW572016 (Lapatinib): relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells.[J]. Cancer research, 2004, 64 18: 6652-6659. DOI:10.1158/0008-5472.can-04-1168
[4] G. GREVE. The pan-HDAC inhibitor panobinostat acts as a sensitizer for erlotinib activity in EGFR-mutated and -wildtype non-small cell lung cancer cells[J]. BMC Cancer, 2015, 15 1. DOI:10.1186/s12885-015-1967-5
[5] JOAN MINGUET  Peter B  Katherine H Smith. Targeted therapies for treatment of non-small cell lung cancer—Recent advances and future perspectives[J]. International Journal of Cancer, 2015, 138 11: 2549-2561. DOI:10.1002/ijc.29915

Erlotinib hydrochloride synthesis

183321-74-6
183319-69-9
Synthesis of Erlotinib hydrochloride from Erlotinib

Erlotinib hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Erlotinib

Erlotinib hydrochloride Suppliers

Global( 794)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Yanxi Chemical Co., Ltd. 		+8618531123677 faithe@yan-xi.com China 5853 58
Hebei Chuanghai Biotechnology Co., Ltd 		+8615531151365 mina@chuanghaibio.com China 18126 58
Anhui Ruihan Technology Co., Ltd 		+8617756083858 daisy@anhuiruihan.com China 973 58
Henan Fengda Chemical Co., Ltd 		+86-371-86557731 +86-13613820652 info@fdachem.com China 20124 58
Shaanxi TNJONE Pharmaceutical Co., Ltd 		+8618092446649 sarah@tnjone.com China 1143 58
Apeloa production Co.,Limited 		+8619933239880 admin@apcl.com.cn China 861 58
BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD. 		+86-18600796368 sales@sjar-tech.com China 529 58
Frapp's ChemicalNFTZ Co., Ltd. 		+86 (576) 8169-6106 sales@frappschem.com China 880 50
Capot Chemical Co.,Ltd. 		+86-（0）57185586718; +8613336195806 sales@capot.com China 29640 60
Beijing Cooperate Pharmaceutical Co.,Ltd 		010-60279497 sales01@cooperate-pharm.com CHINA 1803 55
Supplier Advantage
Hebei Yanxi Chemical Co., Ltd. 		58
Hebei Chuanghai Biotechnology Co., Ltd 		58
Anhui Ruihan Technology Co., Ltd 		58
Henan Fengda Chemical Co., Ltd 		58
Shaanxi TNJONE Pharmaceutical Co., Ltd 		58
Apeloa production Co.,Limited 		58
BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD. 		58
Frapp's ChemicalNFTZ Co., Ltd. 		50
Capot Chemical Co.,Ltd. 		60
Beijing Cooperate Pharmaceutical Co.,Ltd 		55

Related articles

View Lastest Price from Erlotinib hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Erlotinib hydrochloride pictures 2026-05-18 Erlotinib hydrochloride
183319-69-9
 0.99 RongNa Biotechnology Co.,Ltd
Erlotinib Hydrochloride pictures 2026-05-18 Erlotinib Hydrochloride
183319-69-9
 US $0.00 / g 1g More Than 99% 100kg/Month BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
Erlotinib hydrochloride pictures 2026-05-18 Erlotinib hydrochloride
183319-69-9
 US $0.00 / Kg/Bag 1KG 99%min 100KGS WUHAN FORTUNA CHEMICAL CO., LTD

Erlotinib hydrochloride Spectrum

Erlotinib hydrochloride(183319-69-9)1HNMR

183319-69-9(Erlotinib hydrochloride )Related Search:

(Trifluoromethoxy)benzene Anisole Topotecan hydrochloride Guaiacol Bis(2-ethylhexyl)amine
Ethoxyquin Triethanolamine Ethoxyethyne 4-Methoxyphenol Nilotinib
Ethoxyamine hydrochloride p-Anisaldehyde Triallylamine Dibenzylamine Triethylamine
ERLOTINIB MESYLATE Erlotinib iMpurity 2 Erlotinib D6 HCl

1of4

ERLOTINIB HCL SALT ERLOTINIB HCL SALT :TARCEVA N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine, Hydrochloride Salt, OSI 774, Tarceva N-(3-Ethynylphenyl)-6,7-bis-(2-methoxyethoxy)-quinazolin-4-amine [6,7-Bis-(2-methoxy-ethoxy)-quinazolin-4yl]-(3-ethynyl-phenyl)-amine Tarceva Hydrochloride See E625000 6,7-Bis(2-methoxyethoxy)-4-(3-ethynylanilino)quinazoline hydrochloride Erlotinib hydrochloride N-(3-Ethynylphenyl)[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amine hydrochloride Erlotinib HCl(TINIBS) erlotinib hydorchloride 6,7-BIS(2-METHOXYETHOXY)-4-(3-ETHYNYLANILINO)QUINAZOLINE HCL Erlotonid HCl 6,7-Bis(2-methoxyethoxy)-4-(3- 21 Erlotinib hydrochloride and Intermediate -(3-Ethynylphenyl)[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amine hydrochloride Erlotinib, Hydrochloride (Tarceva Hydrochloride) Tarceva Hydrochloride (Erlotinib Hydrochloride) Erlotinib Hydrochloride (Tarceva) Erlotinib, OS-774 4-(m-Ethynylanilino)-6,7-bis(2-methoxyethoxy)quinazoline monohydrochloride Tarceva (Erlotinib Hydrochloride) 4-QuinazolinaMine, n-(3-ethynylphenyl)-6,7-bis(2-Methoxyethoxy)-, hydrochloride Erlotinib HCL and InterMediate 4-QuinazolinaMine,N-(3-ethynylphenyl)-6,7-bis(2-Methoxyethoxy)-,hydrochloride(1:1) [6,7-Bis(2-Methoxyethoxy)quinazolin-4-yl]-(3-ethynylphenyl)aMine Hydrochloride CP 358774 N-(3-Ethynylphenyl)-6,7-bis(2-Methoxyethoxy)-4-quinazolinaMine Hydrochloride OSI 774 NSC718781 OSI774;CP-358774;TARCEVA;NSC718781 [6,7-Bis-(2-Methoxy-ethoxy)-quinazolin-4-yl]-(3-ethynyl-phenyl)-aMine.HCl N-(3-Ethynylphenyl)-6,7-bis(2-Methoxyethoxy)quinazolin-4-aMine hydrochloride Erlotinib Hydrochlorid Erlotinib-d6 HCl Erlotinib hydrochloride (SynonyMs CP-358774, OSI-774, NSC 718781) CP-358774-01 RG-1415 RO-0508231 Erlotinib HCl (OSI-744) Erlotinib hydrochloride, 98.5% Tarceva, CP-358774 Erlotinib Hydrochloride WS NSC 718781) HCl Erlotinib hydrochloride N-(3-Ethynylphenyl)[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amine hydrochloride Erlotinib HCl, >=99% Erlotinib hydrochlroide Erlotinib (OSI-744) HCl Erlotinib Hcl(CP-358) N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)quizolin-4-amine CS-491 Erlotinib-11 Erlotinib Hydrochloride iMpurity 10 Erlotinib (OSI-744) hydrochloride otinib hydrochL Erlotinib hydrochloride USP/EP/BP erlotinib high quali Erlotinib hydrochloride (API)