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7-Azaindole

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7-Azaindole Basic information
Product Name:7-Azaindole
Synonyms:1,7-Diaza-1H-indene;7-Aza-7H-indole;7-Aza-1-pyrindine;7H-Pyrrolo[2,3-b]pyridine;Pyrrolo(2,3-b)pyridine;7-AZAINDOLE CRYSTALLINE;7-AZAINDOLE 98%;7-Azaindole99%
CAS:271-63-6
MF:C7H6N2
MW:118.14
EINECS:205-981-0
Product Categories:blocks;IndolesOxindoles;Heterocycles;Indole Derivatives;Pharmaceutical intermediate;Heterocycles series;Indole;Heterocyclic Compounds;Indole Series;Heterocycle-Indole series;Heterocycle-Pyridine series;buildingblock;Halogenated Heterocycles ,Thiazoles;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:271-63-6.mol
7-Azaindole Structure
7-Azaindole Chemical Properties
Melting point 105-107 °C (lit.)
Boiling point 270 °C (753.1004 mmHg)
density 1.1151 (rough estimate)
refractive index 1.5500 (estimate)
Fp 270°C
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, Methanol
pka7.69±0.20(Predicted)
form Powder
color White to off-white
BRN 109667
InChIKeyMVXVYAKCVDQRLW-UHFFFAOYSA-N
CAS DataBase Reference271-63-6(CAS DataBase Reference)
NIST Chemistry Reference1H-Pyrrolo[2,3-b]pyridine(271-63-6)
EPA Substance Registry System1H-Pyrrolo[2,3-b]pyridine (271-63-6)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36-41-37/38-22
Safety Statements 39-26-36/37/39
WGK Germany 3
RTECS UY8710000
HazardClass IRRITANT
HS Code 29339990
MSDS Information
ProviderLanguage
1H-Pyrrolo[2,3-b]pyridine English
SigmaAldrich English
ACROS English
ALFA English
7-Azaindole Usage And Synthesis
Chemical PropertiesBrown-Cyrstalline Solid
Uses7-Azaindole is imidazolinone derivatives as CGRP receptor antagonists used in the treatment.
A heterocyclic molecule that can be utilized as a pharmaceutical building block.
Starting material in a recent synthesis of azaserotonin.
Application7-Azaindole is a heterocyclic organic compound, which is an organic synthesis intermediate and a pharmaceutical intermediate. It is the core structure of many drugs, such as antitumor drugs, dopamine D4 receptors, p38 kinase inhibitors, thrombin inhibitors, etc.
PreparationSynthesis of 7-azaindole: in a single-necked flask, add 2.0 g of 2-amino-3-methylpyridine and 2.5 g of N-Methylformanilide into 40 mL of dichloromethane, and add 3.15 g of PCl with stirring under an ice-water bath. After 4 hours of reaction, the reaction system was slowly poured into 40 mL of ammonia water, and the insoluble matter was removed by suction filtration. The organic layer was separated, washed twice with water, dried over anhydrous sodium sulfate, and evaporated to dryness to obtain 2.91 g of 7-azaindole as a pale yellow solid, with a yield of 70%.
DefinitionChEBI: 1H-pyrrolo[2,3-b]pyridine is a pyrrolopyridine.
Purification MethodsRecrystallise it repeatedly from EtOH, then sublime it in a vacuum [Tokumura et al. J Am Chem Soc 109 1346 1987]. The N-acetate has m 65-66o (from *C6H6), and the picrate has m 232-233o (from Me2CO) [Clemo & Swan J Chem Soc 603 1945, Beilstein 23 III/IV 1105.]
Tag:7-Azaindole(271-63-6) Related Product Information
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