참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Sodium Cyanate | HCID 517096 | — |
| 반응물 | 5-Bromothiazol-2-amine monohydrobromide | HCID 2723848 | — |
| 반응물 | 2,6-Dimethylbiphenyl-4-sulfonyl chloride | HCID 86616717 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-[(5-bromo-1,3-thiazol-2-yl)carbamoyl]-2,6-dimethylbiphenyl-4-sulfonamide | HCID 24752210 | 9% |
반응 단계
2,6-Dimethylbiphenyl-4-sulfonyl chloride (0.147 g, 0.53 mmol, 1.4 equiv.) and pyridine (0.152 ml, 1.87 mmol, 5.0 equiv.) were added to a stirred suspension of sodium cyanate (56 mg, 0.86 mmol, 2.3 equiv.) in dry acetonitrile (1.5 ml) and the mixture stirred at room temperature for 3 hours. 5-Bromo-thiazol-2-ylamine hydrobromide (97 mg, 0.38 mmol, 1.0 equiv.) was added and the reaction stirred for 1 hour. Water (2 ml) and acetic acid (3 drops) were added. The product was extracted into dichloromethane (2 ml), dried over sodium sulfate and evaporated to a brown gum. The gum was purified by preparative HPLC to give N-[(5-bromo-1,3-thiazol-2-yl)carbamoyl]-2,6-dimethylbiphenyl-4-sulfonamide, 15 mg (9% yield). LC @UV215 nm; Rt 2.64: 96%, m/z (ES+): 467, 468 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07868030B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-e60926281d7f4260a3e48e4d53bf8663 |
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| 출처 메모 | uspto-grants-2011_01 |
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