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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1162748생성일: 2026년 10월 25일

1,1'-Carbonyldiimidazole → 2-(2-(3-(Trifluoromethyl)-4,5,6,7-tetrahydroindazole-1-yl)acetamido)thiophene-3-carboxamide

https://huagongshe.com/reaction/1162748

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물2-Aminothiophene-3-carboxamideHCID 699495—
반응물[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]acetic acidHCID 788039—
용매dichloromethane N,N-dimethylformamideHCID 22350042—
생성물2-(2-(3-(Trifluoromethyl)-4,5,6,7-tetrahydroindazole-1-yl)acetamido)thiophene-3-carboxamideHCID 529415022%

반응 조건

온도120 °C

반응 단계

2-aminothiophene-3-carboxamide (23 mg, 0.16 mmol) and 2-(3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole-1-yl)acetic acid (40 mg, 0.16 mmol) were dissolved in DCM/DMF (2 mL/50 μL) and polymer supported carbonyldiimidazole (264 mg, 1.2 mmol/g, 0.32 mmol) added. The reaction mixture was heated at 120° C. for 10 min in a Biotage SmithCreator microwave. The reaction mixture was filtered washing with MeOH (10 mL), EtOAc (10 mL), and MeCN (10 mL). The filtrate was concentrated in vacuo to give a yellow gum. Purification by preparative reverse phase HPLC gave desired product (1 mg, 2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07820707B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-31b1677b6eee4b349fa72a597452b90c
출처 메모uspto-grants-2010_10