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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 884596생성일: 2026년 10월 26일

4-Bromobutyryl chloride → 5-{6-[(4-Bromo-butyrylamino)-methyl]-pyrimidin-4-yloxy}-indole-1-carboxylic acid (4-fluoro-3-trifluoromethyl-phenyl)-amide

https://huagongshe.com/reaction/884596

반응식

참여 물질

역할이름HCID투입량
반응물4-Bromobutyryl chlorideHCID 70225—
반응물DiisopropylethylamineHCID 81531—
반응물5-(6-Aminomethyl-pyrimidin-4-yloxy)-indole-1-carboxylic acid (4-fluoro-3-trifluoromethyl-phenyl)-amideHCID 59394236—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물5-{6-[(4-Bromo-butyrylamino)-methyl]-pyrimidin-4-yloxy}-indole-1-carboxylic acid (4-fluoro-3-trifluoromethyl-phenyl)-amideHCID 59394487—

반응 단계

5-(6-Aminomethyl-pyrimidin-4-yloxy)-indole-1-carboxylic acid (4-fluoro-3-trifluoromethyl-phenyl)-amide (52.5 mg, 0.117 mmol) is dissolved in DCM (5 mL) at 0° C. DIEA (0.025 mL, 0.143 mmol) is added followed by 4-bromo-butyryl chloride (0.020 mL, 0.172 mmol). The reaction is stirred for 30 min before being diluted with ethyl acetate and washed with water. The organic layer is removed, dried, and concentrated to provide the title compound. MS (ESI) m/z 595.6 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08242125B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-2590b25cb7974e77af4d61930d5d801f
출처 메모uspto-grants-2012_08