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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 450242생성일: 2026년 10월 26일

3-(Trifluoromethyl)phenyl isocyanate → 5-methyl-4-[1-(3-trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-5,7-dihydro-pyrrolo[3,4-d]pyrimidine-6-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/450242

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물tert-butyl 4-(1H-indol-5-yloxy)-5-methyl-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylateHCID 59394355—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5-methyl-4-[1-(3-trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-5,7-dihydro-pyrrolo[3,4-d]pyrimidine-6-carboxylic acid tert-butyl esterHCID 59394477—

반응 단계

To a solution of 4-(1H-Indol-5-yloxy)-5-methyl-5,7-dihydro-pyrrolo[3,4-d]pyrimidine-6-carboxylic acid tert-butyl ester (400 mg, 1.092 mmol) in THF (10 mL) at 0° C., sodium hydride (74.2 mg, 1.856 mmol, 60% in mineral oil) is added. After 10 min, 1-isocyanato-3-trifluoromethyl-benzene (0.314 ml, 2.183 mmol) is added and the reaction is allowed to reach rt. After 2 h, a saturated solution of NH4Cl in water (5 mL) is added. The organics are extracted with EtOAc (×3), dried and evaporated to give the crude 5-methyl-4-[1-(3-trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-5,7-dihydro-pyrrolo[3,4-d]pyrimidine-6-carboxylic acid tert-butyl ester. MS (ESI) m/z 554.9 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486954B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-d20e2dab3c07472eb5e4436502a58304
출처 메모uspto-grants-2013_07