Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 538037생성일: 2026년 10월 24일
Dichloromethane → [4-(4-Isobutyryl-piperazine-1-carbonyl)-cyclohexylmethyl]-carbamic acid tert-butyl ester
https://huagongshe.com/ko/reaction/538037
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | 2-Methyl-1-(piperazin-1-yl)propan-1-one | HCID 2761409 | — |
| 반응물 | HCID 178453624 | HCID 178453624 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | [4-(4-Isobutyryl-piperazine-1-carbonyl)-cyclohexylmethyl]-carbamic acid tert-butyl ester | HCID 67114063 | 80.2% |
반응 단계
To a solution of trans-4-(tert-Butoxycarbonylamino-methyl)-cyclohexanecarboxylic acid (8.5 g, 32.8 mmol) in DCM (100 mL) 1,1-carbonyldiimidazole (4.87 g, 30.1 mmol) was added and the reaction was left stirring for 2 hours. Then isobutyryl-piperazine (6.95 g, 27.3 mmol) was also added and the reaction was left stirring for 16 h at room temperature. The mixture was diluted with 50 mL of H2O, the organic phase collected and the solvent removed under reduced pressure. The residue was washed with 1N NaOH solution and the precipitate was filtered, affording 8.7 g (21.9 mmol) of [4-(4-Isobutyryl-piperazine-1-carbonyl)-cyclohexylmethyl]-carbamic acid tert-butyl ester. The product obtained was dissolved in 100 mL of DCM and H2SO4 (2.92 mL, 54.9 mmol) was added. The reaction was stirred for 18 hours and the mixture was washed with 50 mL of 15% NaOH solution, the organic phase was collected and concentrated under reduced pressure. 3.85 g of the titled product were obtained (yield=48%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08865704B2 |
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| 출처 데이터셋 | uspto-grants-2014_10 |
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| ORD ID | ord-d17cb512b72747cb8ce63f46cdf5b15e |
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| 출처 메모 | uspto-grants-2014_10 |
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