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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45134생성일: 2026년 10월 24일

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/ko/reaction/45134

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 번호US08541432B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-957f92fc0b514c5a9ed5ca74bdf74659
출처 메모uspto-grants-2013_09