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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490446생성일: 2026년 10월 24일

Acetic Acid → 5-chloro-2-(5,6-dimethoxy-1-methyl-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/ko/reaction/490446

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Potassium tert-butoxideHCID 23665647—
반응물5-chloro-3-(5,6-dimethoxy-1-methyl-1H-indol-3-ylethynyl)pyridin-2-ylamineHCID 67147644—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물5-chloro-2-(5,6-dimethoxy-1-methyl-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyridineHCID 4686816263.6%

반응 조건

온도70 °C

반응 단계

A suspension of 0.44 g of 5-chloro-3-(5,6-dimethoxy-1-methyl-1H-indol-3-ylethynyl)pyridin-2-ylamine and 0.58 g of potassium tert-butoxide in 25 ml of 1-methylpyrrolidin-2-one is heated at a temperature in the region of 70° C. for approximately 4 hours 30 minutes. The mixture is concentrated to dryness under reduced pressure (13 kPa). The residue is taken up with 40 ml of water and the pH of the suspension obtained is brought to approximately 4-5 by adding glacial acetic acid. After agitation for approximately 10 minutes, the solid is filter-dried, washed with three times 5 ml of water and then air-dried. After recrystallization from 160 ml of propan-1-ol, 0.28 g of 5-chloro-2-(5,6-dimethoxy-1-methyl-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyridine is obtained in the form of a beige solid, the characteristics of which are as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528147B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-fe508c895b1d46958f6ae767c0b9640b
출처 메모uspto-grants-2009_05