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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1162750생성일: 2026년 10월 25일

Potassium Iodide → 2-(2-(3-(Trifluoromethyl)-4,5,6,7-tetrahydroindazole-1-yl)propanamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

https://huagongshe.com/reaction/1162750

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium hydrideHCID 24758—
반응물2-(3-Chloropropanamido)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamideHCID 1666398—
반응물3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazoleHCID 2802863—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(2-(3-(Trifluoromethyl)-4,5,6,7-tetrahydroindazole-1-yl)propanamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamideHCID 6864789920%

반응 단계

3-(trifluoromethyl)-4,5,6,7-tetrahydroindazole (50 mg, 0.263 mmol) was dissolved in DMF (2 mL). NaH (60% [w/w] suspension in oil, 11 mg, 0.275 mmol) was added followed by potassium iodide (2 mg, catalyst) and the reaction mixture stirred at RT for 30 min. 2-(3-chloropropanamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide (75 mg, 0.262 mmol) was then added and the reaction mixture heated at 120° C. for 400 sec in a Biotage SmithCreator microwave. Water was added followed by EtOAc (3×10 mL) extraction. The EtOAc layers were washed with water (5×5 mL), brine, dried over MgSO4, filtered and the solvent removed in vacuo to give a yellow gum. Purification by preparative reverse phase HPLC gave desired product (22.7 mg, 0.052 mmol, 20%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07820707B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-9fcb980c4b0c40ada260e2c055f276c5
출처 메모uspto-grants-2010_10