돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus trichlorideHCID 24387—
반응물2-Chloro-3-pyridylamineHCID 80528—
반응물3-Acetamidothiophene-2-carboxylic acidHCID 2807579—
용매PyridineHCID 1049—
생성물2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-oneHCID 1835067963%

반응 조건

온도105 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323208B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-2d0269e9bbed4ddebd146f92e46f6348
출처 메모uspto-grants-2001_11