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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20273생성일: 2026년 10월 26일

4-Chloroaniline → tert-Butyl 4-{[(4-chlorophenyl)amino]carbonyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/20273

반응식

참여 물질

역할이름HCID투입량
반응물4-ChloroanilineHCID 7812—
반응물TriethylamineHCID 8471—
반응물1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매AcetonitrileHCID 6342—
생성물tert-Butyl 4-{[(4-chlorophenyl)amino]carbonyl}piperidine-1-carboxylateHCID 29201912—

반응 단계

1-BOC-piperidine-4-carboxylic acid (100 g, 437 mmol), 4-chloroaniline (61.2 g, 480 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (100 g, 524 mmol) and triethylamine (182.6 mL, 1.31 mol) were dissolved in cold (10° C.) acetonitrile (1.75 L). The reaction mixture was stirred for 54 hours at room temperature and then concentrated under reduced pressure. The residue was dissolved in ethyl acetate and then partitioned with 2N hydrochloric acid. The resulting precipitate was filtered off, re-dissolved in dichloromethane, the solution was dried over MgSO4 and evaporated under reduced pressure. The residue was triturated with ether to afford the desired compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745630B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-41a1e14ffd1d4ff2a1dd973b7f136e76
출처 메모uspto-grants-2010_06