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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 445340생성일: 2026년 10월 24일

Water → (R)-N-(3-Cyano-4-fluorophenyl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydro-isoquinoline-2(1H)-carboxamide

https://huagongshe.com/reaction/445340

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물5-Amino-2-fluorobenzonitrileHCID 2737673—
반응물(R)-4-Nitrophenyl 1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 59536297—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물(R)-N-(3-Cyano-4-fluorophenyl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydro-isoquinoline-2(1H)-carboxamideHCID 59536324—

반응 단계

A solution of 5-amino-2-fluorobenzonitrile (62 mg, 452 μmol) and sodium hydride, 60% dispersion in mineral oil (26 mg, 678 μmol) in THF (1.0 mL) was stirred at RT for 15 min. Then, (R)-4-nitrophenyl 1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate (100 mg, 226 μmol, example 88) was added and the mixture was stirred at RT for overnight. Then, a solution of H2O and MeOH (1:1, 0.2 mL) was added and the solvents were removed. The residue was then dissolved in a solution of DMSO and MeOH (1:1, 1 mL). The solution mixture was then purified by preparative HPLC (0%-100% MeCN 0.1% TFA/H2O 0.1% TFA) to give the desired product, which was dissolved in MeOH (1 mL). The solution was then washed through PL-HCO3 MP resin (polymerlabs, 200 mg/6 mL tube) and the resin was washed with MeOH (2×0.5 mL). The combined washings were then concentrated and dried under vacuum to give the title compound as an orange solid. MS (ESI, positive ion) m/z: 440 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08476297B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-2394235fc9e54306b053e878abef2057
출처 메모uspto-grants-2013_07