참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Aminobenzoic Acid | HCID 978 | — |
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Ethylenediamine | HCID 3301 | — |
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | 2,6-Dimethylaniline | HCID 6896 | — |
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Ameltolide | HCID 13086 | 72.7% |
반응 단계
Oxalyl chloride (1.9 mL, 22 mmol) was added dropwise to a solution of DMF (1.7 mL, 22 mmol) and DCM (22 mL) that was kept at 0° C. The resulting foamy white suspension was stirred for 30 min and allowed to warm to room temperature, then cooled again to 0° C. 4-Aminobenzoic acid (1.50 g, 10.9 mmol) was added and the reaction mixture was stirred at room temperature for 1 h. The flask was again cooled to 0° C. and DCM (11 mL) and pyridine (2.6 mL, 33 mmol) were added. Stirring was continued for 50 min and 2,6-dimethyl-phenylamine (1.33 g, 10.9 mmol) was then added. The reaction mixture was stirred at room temperature for 1.5 h and concentrated to dryness. The residue was dissolved in ethanol (30 mL) and 1,2-ethylenediamine (3.3 mL, 49 mmol) was added. The reaction mixture was heated at reflux for 2 h, allowed to cool to room temperature, stirred for 2 d, and concentrated. Water (50 mL) was added to the residue and the precipitate was collected, rinsed well with water, and dried to yield the titled compound (1.904 g, 70% yield). MS (ESI/Cl): mass calcd. for C15H16N2O, 240.1; m/z found, 241.1 [M+H]+. 1H NMR (400 MHz, CD3OD): 7.76 (d, J=8.8 Hz, 2H), 7.10 (s, 3H), 6.72 (d, J=8.8 Hz, 2H), 2.24 (s, 6H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08937078B2 |
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| 출처 데이터셋 | uspto-grants-2015_01 |
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| ORD ID | ord-c1ba85ab04744ab6954e5c61f54177ee |
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| 출처 메모 | uspto-grants-2015_01 |
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