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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401824생성일: 2026년 10월 26일

Hydrochloric Acid → 4-Amino-N-{[1-(4-chlorophenyl)cyclopropyl]methyl}-3-fluorobenzamide

https://huagongshe.com/reaction/401824

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylformamideHCID 6228—
반응물4-Amino-3-fluorobenzoic acidHCID 9971—
반응물DiisopropylethylamineHCID 81531—
반응물[1-(4-Chlorophenyl)cyclopropyl]methanamineHCID 4120166—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
생성물4-Amino-N-{[1-(4-chlorophenyl)cyclopropyl]methyl}-3-fluorobenzamideHCID 57732017—

반응 단계

To a mixture of 4-amino-3-fluorobenzoic acid (180.0 mg, 1.160 mmol) and N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (HATU, 0.44 g, 1.2 mmol) in N,N-dimethylformamide (2 mL, 20 mmol) at 0° C. were added N,N-diisopropylethylamine (0.61 mL, 3.5 mmol) and C-[1-(4-chloro-phenyl)-cyclopropyl]-methylamine; hydrochloride (303.7 mg, 1.392 mmol). The reaction mixture was slowly warmed to rt. The reaction mixture was quenched with an equal volume of saturated aqueous sodium bicarbonate and extracted with ethyl acetate (3×). The combined organic layers were washed successively with water, aqueous lithium chloride, and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified on the Isco (120 g cartridge, chloroform to 12% methanol in chloroform).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741934B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-84fb4d19c7494da498e16b1b3afaa9c4
출처 메모uspto-grants-2014_06