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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550831생성일: 2026년 10월 26일

Trifluoroacetic acid → 1-[2-(4-Fluoro-3-trifluoromethyl-benzylamino)-ethyl]-3-(7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-urea

https://huagongshe.com/reaction/550831

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물TriethylamineHCID 8471—
반응물4-Fluoro-3-(trifluoromethyl)benzaldehydeHCID 522269—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물3-Amino-pyrrolidine-1-carboxylic acid (7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-amideHCID 72489372—
용매MethanolHCID 887—
생성물1-[2-(4-Fluoro-3-trifluoromethyl-benzylamino)-ethyl]-3-(7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-ureaHCID 5901197118.1%

반응 조건

온도25 °C

반응 단계

A solution of the trifluoroacetic acid salt of 3-amino-pyrrolidine-1-carboxylic acid (7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-amide (176 mg, 0.46 mmol) in methanol (6 ml), 4-fluoro-3-(trifluoromethyl) benzaldehyde (90 mg, 0.46 mmol) and sodium triacetoxyborohydride (293 mg, 1.38 mmol) at 25° C. The resulting solution was stirred at 25° C. overnight. At this time, the reaction mixture was treated with triethylamine (200 mL, 1.44 mmol) and then was stirred for an additional 24 h. At this time, the reaction was concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, gradient elution 95/5 methylene chloride/methanol) afforded 1-[2-(4-fluoro-3-trifluoromethyl-benzylamino)-ethyl]-3-(7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-urea (37 mg, 18%); ES-HRMS m/e calcd for C17H16F4N6O2S (M+H)+ 445.1065, found 445.1065.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947692B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-ba39de26c4c24720851a8cbd412f5c07
출처 메모uspto-grants-2011_05