Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430511생성일: 2026년 10월 26일
Phosphorus trichloride → 2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-one
https://huagongshe.com/reaction/430511
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Phosphorus trichloride | HCID 24387 | — |
| 반응물 | 2-Chloro-3-pyridylamine | HCID 80528 | — |
| 반응물 | 3-Acetamidothiophene-2-carboxylic acid | HCID 2807579 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-one | HCID 18350679 | 63% |
반응 단계
To a mixture of pyridine (4 mL), 3-amino-2-chloropyridine (0.514 g, 4 mmol), and 3-acetamidothiophene-2-carboxylic acid (0.370 g, 4 mmol) was added phosphorus trichloride (0.02 mL, 2.3 mmol). The reaction was heated to 105° C. for 3 hours, cooled to ambient temperature and partitioned between ethyl acetate and water. Phases were separated and the aqueous layer was extracted with ethyl acetate. The combined organic phase was washed with water and brine, dried over sodium sulfate and concentrated to a greenish brown oil. This residue was flash chromatographed on silica gel (20×120 mm) eluting with 20-40% ethyl acetate/hexane to afford 0.350 g (63%) of 2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-one as a yellow foam.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06323208B1 |
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| 출처 데이터셋 | uspto-grants-2001_11 |
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| ORD ID | ord-2d0269e9bbed4ddebd146f92e46f6348 |
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| 출처 메모 | uspto-grants-2001_11 |
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