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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220907생성일: 2026년 10월 24일

4-Chloro-N-methylbenzenamine → 4-(3-{4-[(4-Chloro-phenyl)-methyl-carbamoyl]-2-fluoro-phenoxy}-propyl)-piperazine-1-carboxylic Acid Tert-butyl Ester

https://huagongshe.com/ko/reaction/220907

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-N-methylbenzenamineHCID 70272—
반응물PyBroPHCID 2733179—
반응물4-[3-(4-Carboxy-2-fluoro-phenoxy)-propyl]-piperazine-1-carboxylic Acid Tert-butyl EsterHCID 57555209—
용매DichloromethaneHCID 6344—
용매DiisopropylethylamineHCID 81531—
생성물4-(3-{4-[(4-Chloro-phenyl)-methyl-carbamoyl]-2-fluoro-phenoxy}-propyl)-piperazine-1-carboxylic Acid Tert-butyl EsterHCID 5755527341%

반응 단계

PyBroP (606 mg, 1.3 mmol) was added to a solution of 4-[3-(4-carboxy-2-fluoro-phenoxy)-propyl]-piperazine-1-carboxylic acid tert-butyl ester from Example E39 (382 mg, 11.0 mmol) in dichloromethane (20 ml) and DIEA (to pH9). The mixture was stirred for 1 h at room temperature then (4-chloro-phenyl)-methyl amine (156 mg, 1.1 mmol) was added. The mixture was stirred for 2 days at room temperature then solvents were concentrated in vacuo. The residue was dissolved in EtOAC, washed with saturated NaHCO3 then brine, dried and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant; EtOAc) to yield the title compound (210 mg, 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202858B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-59342acd21c4412db3be6a29284765f2
출처 메모uspto-grants-2012_06