참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 2-Aminobenzene-1,3-dicarboxamide | HCID 10241384 | — |
| 반응물 | 2-Propoxybenzoyl chloride | HCID 15921913 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 8-Carbamoyl-2-(2-n-propoxyphenyl)quinazolin-4(3H)-one | HCID 135985156 | 40% |
반응 단계
2-n-Propoxybenzoyl chloride (7.27 g, 0.366 mol) was added dropwise to a stirred suspension of 2-amino-3-carbamoylbenzamide (Preparation 17; 2.63 g, 0.0147 mol) in pyridine (50 ml) at 0° C. The mixture was stirred at room temperature for 3 days, then the solvent evaporated under vacuum. The residue was treated with water (100 ml) and, on chilling the solution, colorless crystals formed. The product was collected by filtration and then suspended in a stirred mixture of sodium hydroxide (1.73 g, 0.043 mol), water (90 ml) and ethanol (20 ml). The mixture was heated under reflux for 3 hours, allowed to cool and filtered. The filtrate was acidified to pH 2 with concentrated hydrochloric acid and extracted with a methanol-dichloromethane mixture (2:98, 3×100 ml). The organic extracts were combined, washed sequentially with saturated aqueous sodium carbonate solution (3×100 ml) and brine (3×50 ml), dried (Na2SO4) and evaporated under vacuum. Crystallization of the residue from ethyl acetate-methanol gave the title compound as a white solid (1 g, 40%), m.p. 226-227° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06562830B1 |
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| 출처 데이터셋 | uspto-grants-2003_05 |
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| ORD ID | ord-9647eecc6d814232a5ed24039f001f77 |
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| 출처 메모 | uspto-grants-2003_05 |
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