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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23617생성일: 2026년 10월 24일

4-Chlorobenzylamine → N-(4-chlorobenzyl)-2-(hydroxymethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide

https://huagongshe.com/ko/reaction/23617

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorobenzylamineHCID 66036—
반응물Sodium MethoxideHCID 10942334—
반응물Ethyl 2-(hydroxymethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylateHCID 22574311—
용매MethanolHCID 887—
생성물N-(4-chlorobenzyl)-2-(hydroxymethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 2257427869.6%

반응 단계

A solution of ethyl 2-(hydroxymethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylate (627 mg, 2.23 mmol), 4-chlorobenzylamine (2.0 mL, 16.4 mmol), 0.5 M sodium methoxide in methanol (25 mL, 8.92 mmol) and methanol (10 mL) was stirred under nitrogen in a tightly capped 250 mL round bottom flask at 50° C. for 24 hours. The initial solution slowly dropped a thick white precipitate during the reaction. After cooling to room temperature, the mixture was filtered, and the collected solid was washed with methanol and dried in vacuo, leaving a white solid. The crude solid was suspended in boiling methanol (200 mL), cooled to room temperature, and filtered, to give the title compound as a white powder (585 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-9e59478c9ad84d828ec914ab1d191438
출처 메모uspto-grants-2005_02