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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77582생성일: 2026년 10월 24일

Trifluoroacetic acid → HCID 86762769, 화합물

https://huagongshe.com/ko/reaction/77582

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물DiisopropylethylamineHCID 81531—
반응물2-Chloro-5-fluoropyrimidineHCID 583466—
반응물HCID 86762770HCID 86762770—
용매Dimethyl SulfoxideHCID 679—
용매Sodium CarbonateHCID 10340—
생성물HCID 86762769HCID 8676276941%

반응 조건

온도50 °C

반응 단계

A solution of N-[3-[(4aR,7aS)-2-benzamido-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide; 2,2,2-trifluoroacetic acid (150 mg, 254 μmol), 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is heated in dimethyl sulfoxide (5 mL) overnight at 40° C. Additional 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is added and the mixture is heated overnight at 50° C. Additional 5-fluoro-2-chloropyrimidine (68 mg, 51 μmol) and diisopropylethylamine (98 μL, 56 μmol) is added and the mixture is heated overnight at 50° C. for a third night. The reaction is cooled, diluted with saturated aqueous sodium carbonate (50 mL) to give a slurry that is filtered and dried in a vacuum oven at 50° C. for 4 hours to give the title compound (60 mg, 41%). ES/MS (m/e): 449 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841293B1
출처 데이터셋uspto-grants-2014_09
ORD IDord-a8ead401e87b41a0ab024ab02b50ac0d
출처 메모uspto-grants-2014_09