Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → 5-Methyl-thiophene-2-carboxylic acid (7-bromo-4-methoxybenzothiazol-2-yl)-amide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 5-Methylthiophene-2-carbonyl chloride | HCID 2760083 | — |
| 반응물 | 7-Bromo-4-methoxy-1,3-benzothiazol-2-amine | HCID 22283200 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-Methyl-thiophene-2-carboxylic acid (7-bromo-4-methoxybenzothiazol-2-yl)-amide | HCID 86584910 | — |
반응 단계
2-Amino-7-bromo-4-methoxybenzothiazol (2.33 g, 9 mmol) is dissolved in dichloromethane (100 ml) and at 0° C. treated with pyridine (2.2 ml, 27 mmol) and 5-methyl-thiophene-2-carbonyl chloride (2.2 g, 13.5 mmol). The reaction mixture is allowed to warm to room temperature and after stirring for additional 18 h quenched with water (100 ml). After separation of the phases, the aqueous phases are extracted twice with ethyl acetate. The combined organic layers are then washed with brine, dried and avaporated to dryness. Flash chromatography on silica (eluent ethyl acetate/cyclohexane 1:1 to 4:1) and final recrystallization from ethyl acetate affords the product as off-white solid. (34 mg, 69%). MS: m/e=384 (M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07317007B2 |
| 출처 데이터셋 | uspto-grants-2008_01 |
| ORD ID | ord-fba67789ff78464ca8329f1fb3615320 |
| 출처 메모 | uspto-grants-2008_01 |