참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,5-Dimethoxybenzaldehyde | HCID 81747 | — |
| 반응물 | 2-Amino-5-nitrobenzamide | HCID 97665 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 반응물 | Sodium Bisulfite | HCID 23665763 | — |
| 용매 | Dimethylacetamide | HCID 31374 | — |
| 생성물 | 6-amino-2-(3,5-dimethoxy-phenyl)-3H-quinazolin-4-one | HCID 136348062 | — |
반응 단계
A mixture of 2-amino-5-nitro-benzamide (1.81 g, 10.0 mmol), 3,5-dimethoxy-benzaldehyde (1.83 g, 11.0 mmol), sodium hydrogen sulfite (58.5 wt %, 3.94 g, 22.0 mmol), and p-toluenesulfonic acid monohydrate (0.38 g, 2.00 mmol) in N,N-dimethylacetamide (20 mL) was stirred at 150° C. for 17 hours under nitrogen and then cooled to room temperature. Saturated aqueous NaHCO3 (approximately 1 mL) was added. The mixture was stirred at room temperature for 2 hours, then concentrated to dryness. Water (80 mL) was added, stirred for 0.5 hours, and filtered. The solid was air dried. The crude compound was purified by column chromatography (silica gel 230-400 mesh; ethyl acetate as eluent) to give 6-amino-2-(3,5-dimethoxy-phenyl)-3H-quinazolin-4-one as a yellow solid. Yield: 1.50 g (50%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09238640B2 |
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| 출처 데이터셋 | uspto-grants-2016_01 |
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| ORD ID | ord-e939b15943194a47b7530321302338fb |
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| 출처 메모 | uspto-grants-2016_01 |
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