참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 4-(Morpholine-4-carbonyl)aniline | HCID 577815 | — |
| 반응물 | 5-Methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid | HCID 18622509 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(4-Morpholinocarbonylphenyl)-5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxamide | HCID 18622500 | — |
| 생성물 | Diisopropylether ethyl acetate | HCID 22281796 | 315.3% |
반응 단계
A mixture of 5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (1.0 g, 4 mmol), toluene (20 mL), N,N-dimethylformamide (10 drops) and thionyl chloride (1.5 mL, 20 mmol) was heated at 60° C. for 1 h. The solvents were removed in vacuo and the residue, dissolved in methylene chloride (20 mL), was added to a solution of 4-aminobenzoylmorpholine (820 mg, 4 mmol, described in: Deylin J. P. J. Chem. Soc. Perkin Trans I, 1975, 830-841) and triethylamine (800 mg, 8 mmol) in methylene chloride (30 mL) at 5° C. After stirring at 20° C. for 2 h, water was added and the organic phase was separated, dried and the solvent removed in vacuo. The oily residue was crystallized from diisopropyl ether/ethyl acetate affording 1.2 g (73% yield) of the title compound as crystals: mp 186-189° C.; EIMS (70 eV) m/z (relative intensity) 439 (20, M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06313118B1 |
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| 출처 데이터셋 | uspto-grants-2001_11 |
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| ORD ID | ord-717ba65c41b6443da0555ea0645bbe72 |
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| 출처 메모 | uspto-grants-2001_11 |
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