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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31422생성일: 2026년 10월 24일

Bromine → 3-Bromo-N-cyclopropyl-5-fluoro-4-methylbenzamide

https://huagongshe.com/ko/reaction/31422

반응식

참여 물질

역할이름HCID투입량
반응물BromineHCID 24408—
반응물3-Fluoro-p-toluic acidHCID 67687—
반응물CyclopropylamineHCID 69828—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매IronHCID 23925—
용매Sodium ThiosulfateHCID 24477—
생성물3-Bromo-N-cyclopropyl-5-fluoro-4-methylbenzamideHCID 2191457544%

반응 조건

온도20 °C

반응 단계

3-Fluoro-4-methylbenzoic acid (462 mg, 3.0 mmol) was added to a stirred mixture of bromine (2.31 ml, 45 mmol) and iron powder (252 mg, 4.5 mmol) under nitrogen. The reaction was stirred at 20° C. for 4 hours and then left to stand for 16 hours. Sodium thiosulphate solution (200 ml) was added and the product was extracted into ethyl acetate (3×150 ml). Ethyl acetate extracts were combined and evaporated in vacuo. The crude product (mixture of isomers) was dissolved in dimethylformamide (7 ml). Cyclopropylamine (208 μl, 3.0 mmol), HOBT (405 mg, 3.0 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (575 mg, 3.0 mmol) and DIPEA (525 μl, 3.0 mmol) were added to the stirred solution. The reaction was stirred for 5 hours at 20° C. Solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. Combined ethyl acetate extracts were washed sequentially with aqueous sodium hydrogen carbonate and hydrochloric acid (0.5M), then dried (magnesium sulphate). The ethyl acetate was evaporated in vacuo and the residue was purified by silica biotage chromatography eluting with cyclohexane:ethyl acetate (6: 1) to give 3-bromo-N-cyclopropyl-5-fluoro4methylbenzamide (359 mg, 44%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425555B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-45e89e4db5f24b42a55a018f50bf17e0
출처 메모uspto-grants-2008_09