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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6876생성일: 2026년 10월 23일

Triethylsilane → N-cyclopropyl-2,4-difluoro-5-((2-(pyridin-2-ylamino)thiazol-5-yl)methylamino)benzamide

https://huagongshe.com/ko/reaction/6876

반응식

참여 물질

역할이름HCID투입량
반응물TriethylsilaneHCID 12052—
반응물5-amino-N-cyclopropyl-2,4-difluorobenzamideHCID 21966507—
반응물2-(Pyridin-2-ylamino)thiazole-5-carbaldehydeHCID 22019058—
용매Trifluoroacetic acid methylene chlorideHCID 21863450—
생성물N-cyclopropyl-2,4-difluoro-5-((2-(pyridin-2-ylamino)thiazol-5-yl)methylamino)benzamideHCID 1163273747.3%

반응 단계

A mixture of 2-[pyridin-2-ylamino]-thiazole-5-carbaldehyde (41.0 mg, 0.2 mmol) and 5-amino-N-cyclopropyl-2,4-difluorobenzamide (46.6 mg, 0.22 mmol) in TFA/DCM (1:1, 1 mL) was stirred at RT for 10 min and triethylsilane (0.1 mL) was added. The mixture was stirred for 1 h, then concentrated and the residue was neutralized with NaHCO3 solution and the precipitates occurred. The precipitates were collected, washed with water and dried. The solid was triturated with MeOH and filtered to afford the title compound as a grayish solid (38 mg, 47%). Small amount of solid was boiled in methanol, the mixture was cooled to RT and filtered to afford a white solid. MS m/z 402 (M+H)+. 1H NMR (DMSO-d6) δ 8.23 (d, 1H, J=4.0 Hz), 8.15 (s, 1 H), 7.65 (t, 1 H, J=7.15 Hz), 7.26 (s, 1 H), 7.16 (m, 1 H), 7.01 (d, 1 H, J=8.75 Hz), 6.95 (m, 1 H), 6.89 (t, 1 H, J=7.15 Hz), 6.12 (s 1 H), 4.43 (m, 2 H), 2.79 (m, 1 H), 0.69 (m, 2 H), 0.51 (m, 2 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084160B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-c09aa937df8b486caaee08ce9bc04f1a
출처 메모uspto-grants-2006_08