Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 881985생성일: 2026년 10월 25일
Dimethylformamide → Tert-butyl 4-(1-(3-(cyclopropylmethoxy)-5-methoxybenzamido)ethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/881985
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 반응물 | tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylate | HCID 22647295 | — |
| 반응물 | 3-(2-Cyclopropylethyl)-5-methoxybenzoic acid | HCID 89463753 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Tert-butyl 4-(1-(3-(cyclopropylmethoxy)-5-methoxybenzamido)ethyl)piperidine-1-carboxylate | HCID 89464457 | — |
반응 단계
To a solution of 3-(2-cyclopropylethyl)-5-methoxybenzoic acid (2.4 g, 10.7 mmol) and tert-butyl 4-(1-aminoethyl)piperidine-1-carboxylate (2.4 g, 10.7 mmol) in DMF (40 ml), was added triethyl amine (4.47 ml). After stirring for 10 minutes at room temperature TBTU (5.15 g, 16.1 mmol) was added in portions. The reaction mixture was stirred at room temperature for 2 hours. 100 ml H2O was added and the product was extracted into ethyla acetate. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by using normal phase chromatography eluting with petroleum ether containing 10% ethyl acetate to give tert-butyl 4-(1-(3-(cyclopropylmethoxy)-5-methoxybenzamido)ethyl)piperidine-1-carboxylate (3.0 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08993757B2 |
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| 출처 데이터셋 | uspto-grants-2015_03 |
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| ORD ID | ord-f87213cc2a164907857dba4e43b554d0 |
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| 출처 메모 | uspto-grants-2015_03 |
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