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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 884576생성일: 2026년 10월 25일

Diisopropylethylamine → (+/-)-3-({6-[1-(3-Trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-pyrimidin-4-ylmethyl}-amino)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/884576

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-Boc-3-aminopyrrolidineHCID 2756370—
반응물methanesulfonic acid 6-[1-(3-trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-pyrimidin-4-ylmethyl esterHCID 46224264—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(+/-)-3-({6-[1-(3-Trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-pyrimidin-4-ylmethyl}-amino)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 59394560—

반응 조건

온도60 °C

반응 단계

To the solution of methanesulfonic acid (±)-6-[1-(3-trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-pyrimidin-4-ylmethyl ester (80 mg, 0.158 mmol) in THF (5 mL), 3-amino-pyrrolidine-1-carboxylic acid tert-butyl ester (88 mg, 0.474 mmol) and diisopropylethylamine (61 mg, 0.474 mmol) are added. The resulting solution is stirred at 60° C. overnight. After cooling to rt, the reaction mixture is diluted with EtOAc and washed with water and then brine. The organic layer is dried with anhydrous Na2SO4, filtered, and condensed. The residue is purified by FCC (0-10% MeOH/DCM) to provide the title compound. MS (ESI) m/z 597.2 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08242125B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-c95f537710774310909fb7168e108c72
출처 메모uspto-grants-2012_08