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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430687생성일: 2026년 10월 27일

1,1'-Carbonyldiimidazole → N-tert-butyloxycarbonyl-4-(4-amino-5-chloro-2-methoxyphenylcarbonylaminomethyl)piperidine

https://huagongshe.com/reaction/430687

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
반응물1-Boc-4-(aminomethyl)piperidineHCID 736817—
용매DimethylformamideHCID 6228—
생성물N-tert-butyloxycarbonyl-4-(4-amino-5-chloro-2-methoxyphenylcarbonylaminomethyl)piperidineHCID 1120034880%

반응 단계

1,1′-Carbonyldiimidazole (1.61 g, 9.91 mmol) was added to a solution of 4-amino-5-chloro-2-methoxybenzoic acid (2.0 g, 9.91 mmol) in dimethylformamide (5 ml). After stirring for 5 min. at room temperature, solution of N-tert-butyloxycarbonyl-4-(aminomethyl)piperidine (1.77 g, 8.26 mmol) in dimethylformamide (5 ml) was added and the reaction mixture was heated at 55° C. After 23 h, the product was extracted into ethyl acetate and the organic layer was washed with aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated. Flash chromatography of the crude product with 2:1, ethyl acetate/hexanes as the eluant gave N-tert-butyloxycarbonyl-4-(4-amino-5-chloro-2-methoxyphenylcarbonylaminomethyl)piperidine (2.63 g) as a foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323223B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-b31a7c863d644f85b0bd55bceeb15496
출처 메모uspto-grants-2001_11