참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-(2-Bromoethoxy)-2-ethoxybenzene | HCID 7010183 | — |
| 반응물 | 5-(2-Aminopropyl)-2-methoxybenzenesulfonamide | HCID 13176811 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Tamsulosin | HCID 129211 | 89.8% |
반응 단계
5-(-2-aminopropyl]-2-methoxybenzenesulfonamide (200 g) was dissolved in dimethylformamide (950 ml) and 1-(2-Bromoethoxy)-2-ethoxybenzene (100.3 g) was added. The reaction mixture was heated to 80-85° C. for 4 hours. Dimethylformamide was then distilled off under vacuum. Water (1000 ml) was added to solid residue and the mixture was heated to 80-90° C. under stirring for 2 hours. The mixture was cooled to room temperature. Formed crystals were filtered off and were suspended in water (900 ml). Suspension was heated to 80-90° C. under stirring for 2 hours. Crystals were filtered, washed with water (200 ml) and dried to give tamsulosin base (150 g, 89.8%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06835853B2 |
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| 출처 데이터셋 | uspto-grants-2004_12 |
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| ORD ID | ord-bf6f2e98215b4b97ab98e26369938b7c |
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| 출처 메모 | uspto-grants-2004_12 |
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