N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride

CAS No.
6113-17-3
Chemical Name:
N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride
Synonyms
N-Phenyl-N-(phenylMethyl)-;Histapyrrodin Hydrochloride;Histapyrrodine Hydrochloride;N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride;Histapyrrodin HydrochlorideQ: What is Histapyrrodin Hydrochloride Q: What is the CAS Number of Histapyrrodin Hydrochloride Q: What is the storage condition of Histapyrrodin Hydrochloride Q: What are the applications of Histapyrrodin Hydrochloride
CBNumber:
CB5941126
Molecular Formula:
C19H25ClN2
Molecular Weight:
316.8682
MDL Number:
MFCD28388243
MOL File:
6113-17-3.mol
Last updated:2023-04-23 13:52:06

N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride Properties

Melting point 196-197°
storage temp. Refrigerator
solubility Methanol (Slightly)
form Solid
color Pale Beige to Pale Green
FDA UNII 1W1AQ870ZC

N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC H443500 HistapyrrodineHydrochloride 6113-17-3 250mg $175 2021-12-16 Buy
Usbiological 278943 Histapyrrodine hydrochloride 6113-17-3 100mg $406 2021-12-16 Buy
American Custom Chemicals Corporation API0017112 HISTAPYRRODINE HYDROCHLORIDE 95.00% 6113-17-3 5MG $499.94 2021-12-16 Buy
Product number Packaging Price Buy
H443500 250mg $175 Buy
278943 100mg $406 Buy
API0017112 5MG $499.94 Buy

N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride Chemical Properties,Uses,Production

Originator

Calcistin,Galenus

Uses

Antihistaminic.

Manufacturing Process

3 Methods of producing of N-(β-N-phenyl-N-benzylaminoethyl)pyrrolidine: 1. A mixture of 100 parts of N-p-chloroethyl-N-benzylaniline and 100 parts of freshly distilled pyrrolidine are heated to boiling under reflux cooling for about 10 h. Diluted aqueous caustic soda lye is added to the reaction mixture until it shows an alkaline reaction. The reaction product formed and unchanged pyrrolidine are extracted with ether. The extract thus obtained is a subjected to a distillation. After the ether has evaporated, there is produced N-(β-Nphenyl-N-benzylaminoethyl)pyrrolidine, which boils at from 198° to 205°C under 1 mm pressure.
2. 34 parts of N-β-chloroethylpyrrolidine hydrochloride are dissolved together with 110 parts of N-benzylaniline in 400 parts of alcohol, and the solution is heated to boiling under reflux cooling for 15 h, while adding 0.5 part of copper powder. After filtering off the copper powder and driving off the alcohol, dilute caustic soda solution is added until the solution shows an alkaline reaction, whereupon the oil separated is distilled in vacuum. After a forerun of excess N-benzylaniline, there passes over as a main fraction the N- (β-N-phenyl-N-benzylaminoethyl)pyrrolidine, which boils at between 198° and 205°C under 1 mm pressure (mercury gauge).
3. 34 parts of N-β-chloroethylpyrrolidine hydrochloride are added to a solution of 120 parts of aniline in 500 parts of alcohol and the mixture is heated to boiling under reflux cooling for 12 h. After rendering the mixture alkaline by adding caustic soda solution, the excess aniline is driven off with steam. The N-(β-N-phenylaminoethyl)pyrrolidine left is fractionated in vacuo (boiling point 160° to 165°C), 98 parts of this compound are dissolved in 250 parts of 10% aqueous caustic soda solution and admixed with 65 parts of bensylchloride while vigorously stirring at from 50° to 60°C. The temperature is raised to 80° to 90°C for 1 h and the product worked up as indicated in the preceding examples. There is obtained the N-(β-N-phenyl-N-benzylaminoethyl) pyrrolidine in a 95% yield.
In practice it is usually used as hydrochloride.

Therapeutic Function

Antihistaminic

N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride Suppliers

Global( 11)Suppliers
Supplier Tel Email Country ProdList Advantage
Alfa Chemistry
+1-5166625404 Info@alfa-chemistry.com United States 21317 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15421 60
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 13028896684 sales@rrkchem.com China 55827 58
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44941 58
Shaanxi Dideu Newmaterial Co., Ltd. 029-63373950 15353716720 1052@dideu.com China 10008 58
N-Phenyl-N-(phenylMethyl)- N-benzyl-N-phenylpyrrolidine-1-ethylamine monohydrochloride Histapyrrodine Hydrochloride Histapyrrodin Hydrochloride Histapyrrodin HydrochlorideQ: What is Histapyrrodin Hydrochloride Q: What is the CAS Number of Histapyrrodin Hydrochloride Q: What is the storage condition of Histapyrrodin Hydrochloride Q: What are the applications of Histapyrrodin Hydrochloride 6113-17-3 Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals