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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2299307생성일: 2026년 10월 25일

2,4,6-Trimethylpyridine → N-[(4-chlorophenyl)methyl]-7-methyl-4-oxo-2-(thiomorpholinomethyl)thieno[2,3-b]pyridine-5-carboxamide

https://huagongshe.com/reaction/2299307

반응식

참여 물질

역할이름HCID투입량
반응물2,4,6-TrimethylpyridineHCID 7953—
반응물Methanesulfonyl chlorideHCID 31297—
반응물ThiomorpholineHCID 67164—
반응물N-[(4-chlorophenyl)methyl]-2-(hydroxymethyl)-7-methyl-4-oxo-thieno[2,3-b]pyridine-5-carboxamideHCID 6482399—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-[(4-chlorophenyl)methyl]-7-methyl-4-oxo-2-(thiomorpholinomethyl)thieno[2,3-b]pyridine-5-carboxamideHCID 648240560%

반응 단계

To a solution of N-(4-chlorobenzyl)-2-(hydroxymethyl)-7-methyl-4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxamide (0.300 g) from Example No. 35 in DMF (16 mL) are added DMAP (16 mg), 2,4,6-collidine (0.27 mL), and methanesulfonyl chloride (0.16 mL). The reaction mixture is stirred at room temperature for 2 h and then thiomorpholine (0.83 mL) is added. The mixture is stirred at room temperature for 3 d and is then poured into water (50 mL). The resulting off-white solid is filtered off and recrystallized from ethanol to yield 0.222 g (60%) of the title compound as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06495683B2
출처 데이터셋uspto-grants-2002_12
ORD IDord-d5b8f3e1664f4b5d9d2127923397e6d5
출처 메모uspto-grants-2002_12