1H-ピロロ[2,3-b]ピリジン(271-63-6)

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1H-ピロロ[2,3-b]ピリジン 製品概要
化学名:1H-ピロロ[2,3-b]ピリジン
英語化学名:7-Azaindole
别名: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番号:271-63-6
分子式:C7H6N2
分子量:118.14
EINECS:205-981-0
カテゴリ情報: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
1H-ピロロ[2,3-b]ピリジン
1H-ピロロ[2,3-b]ピリジン 物理性質
融点 105-107 °C (lit.)
沸点 270 °C (753.1004 mmHg)
比重(密度) 1.1151 (rough estimate)
屈折率 1.5500 (estimate)
闪点 270°C
貯蔵温度 Sealed in dry,Room Temperature
溶解性Chloroform, Methanol
酸解離定数(Pka)7.69±0.20(Predicted)
外見 Powder
White to off-white
BRN 109667
InChIKeyMVXVYAKCVDQRLW-UHFFFAOYSA-N
CAS データベース271-63-6(CAS DataBase Reference)
NISTの化学物質情報1H-Pyrrolo[2,3-b]pyridine(271-63-6)
EPAの化学物質情報1H-Pyrrolo[2,3-b]pyridine (271-63-6)
安全性情報
主な危険性 Xi,Xn
Rフレーズ 36-41-37/38-22
Sフレーズ 39-26-36/37/39
WGK Germany 3
RTECS 番号UY8710000
国連危険物分類 IRRITANT
HSコード 29339990
MSDS Information
ProviderLanguage
1H-Pyrrolo[2,3-b]pyridine English
SigmaAldrich English
ACROS English
ALFA English
1H-ピロロ[2,3-b]ピリジン Usage And Synthesis
外観白色~微黄色の結晶又は結晶性粉末
用途有機合成原料。
化学的特性Brown-Cyrstalline Solid
使用7-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.
主な応用7-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.
製造方法Synthesis 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%.
定義ChEBI: 1H-pyrrolo[2,3-b]pyridine is a pyrrolopyridine.
純化方法Recrystallise 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.]
Tags:271-63-6