참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| 반응물 | 2-Methoxy-6-nitrobenzoic acid | HCID 13300035 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-(1-benzyl-piperidin-4-yl)-2-methoxy-6-nitrobenzamide | HCID 21102223 | 86% |
반응 단계
2-Methoxy-6-nitro-benzoic acid (2.0 g, 10.1 mmol), 4-amino-1-benzylpiperidine (1.9 mL, 10.1 mmol), 1-hydroxybenzotriazole (1.43 g, 10.5 mmol) and 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide (1.9 g, 10.1 mmol) were combined in ethyl acetate (25 mL). To this solution was added triethylamine (4.2 mL. 30.3 mmol) and the reaction mixture stirred at 40° C. for 2 h. After cooling to room temperature, the mixture was diluted with ethyl acetate and washed with water (2×), 5% sodium bicarbonate, brine (2×), dried over sodium sulfate, and concentrated to afford 3.2 g (86%) of the desired product. LC/MS: tR=1.10 min, 370.28 (MH)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07842808B2 |
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| 출처 데이터셋 | uspto-grants-2010_11 |
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| ORD ID | ord-2b74055737bb4bd19eff0b79415b2945 |
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| 출처 메모 | uspto-grants-2010_11 |
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