Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68759생성일: 2026년 10월 24일
4-Iodobenzoic acid → 4-[Cyclopropyl-(4-iodo-benzoyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/ko/reaction/68759
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Iodobenzoic acid | HCID 12085 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 반응물 | tert-Butyl 4-(cyclopropylamino)piperidine-1-carboxylate | HCID 2769591 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-[Cyclopropyl-(4-iodo-benzoyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester | HCID 68290220 | — |
반응 단계
2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (2.67 g) is added to a solution of 4-iodo-benzoic acid (2.06 g) and ethyldiisopropylamine (2.88 mL) in N,N-dimethylformamide (15 mL) at room temperature. The solution is stirred for 10 min prior to the addition of 4-cyclopropylamino-piperidine-1-carboxylic acid tert-butyl ester (2.00 g). The resulting mixture stirred at room temperature overnight. The mixture is concentrated in vacuo and the residue is mixed with water and ethyl acetate. The organic phase is separated, washed with water and aqueous NaHCO3 solution, dried, and the solvent is evaporated. The crude product is used for the next reaction step without further purification. LC (method 5): tR=2.32 min; Mass spectrum (ESI+): m/z=471 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822471B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-464cde27ee4d4693b998c15da72b5346 |
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| 출처 메모 | uspto-grants-2014_09 |
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