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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397380생성일: 2026년 10월 25일

Piperidine → 5-(4-chloro-2-oxo-1,2-dihydro-pyrrolo [2,3-b]pyridin-3-ylidenemethyl)-4-methyl-1H-pyrrole-2-carboxylic acid (2-morpholin-4-yl-ethyl)-amide

https://huagongshe.com/reaction/397380

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물4-Chloro-1H-pyrrolo[2,3-B]pyridin-2(3H)-oneHCID 11194563—
반응물5-formyl-4-methyl-1H-pyrrole-2-carboxylic acid (2-morpholin-4-yl-ethyl)-amideHCID 11277086—
용매EthanolHCID 702—
생성물5-(4-chloro-2-oxo-1,2-dihydro-pyrrolo [2,3-b]pyridin-3-ylidenemethyl)-4-methyl-1H-pyrrole-2-carboxylic acid (2-morpholin-4-yl-ethyl)-amideHCID 7016092392%

반응 단계

A reaction mixture of 4-chloro-1,3-dihydro-pyrrolo[2,3-b]pyridin-2-one (85 mg, 0.5 mmol), 5-formyl-4-methyl-1H-pyrrole-2-carboxylic acid (2-morpholin-4-yl-ethyl)-amide (125 mg, 0.5 mmol), 0.1 mL of piperidine and 10 mL of ethanol was stirred at room temperature overnight. The yellow precipitate was filtered after cooled with an ice bath, washed with cold ethanol and dried to give 185 mg (92%) of 5-(4-chloro-2-oxo-1,2-dihydro-pyrrolo[2,3-b]pyridin-3-ylidenemethyl)-4-methyl-1H-pyrrole-2-carboxylic acid (2-morpholin-4-yl-ethyl)-amide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610688B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-46e1ae3ea67549dbb46efb62529df636
출처 메모uspto-grants-2003_08