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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | 4-Amino-5-chloro-2-methoxybenzoic acid | HCID 81626 | — |
| 반응물 | 1-Boc-4-(aminomethyl)piperidine | HCID 736817 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-tert-butyloxycarbonyl-4-(4-amino-5-chloro-2-methoxyphenylcarbonylaminomethyl)piperidine | HCID 11200348 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06323223B1 |
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| 출처 데이터셋 | uspto-grants-2001_11 |
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| ORD ID | ord-b31a7c863d644f85b0bd55bceeb15496 |
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| 출처 메모 | uspto-grants-2001_11 |
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