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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68294생성일: 2026년 10월 24일

Triethylamine → 6-(2-Methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxamide

https://huagongshe.com/ko/reaction/68294

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물PyBOPHCID 2724699—
반응물6-(2-Methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxylic acidHCID 39375279—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물6-(2-Methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxamideHCID 58872649—

반응 단계

To a stirred suspension of 6-(2-methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxylic acid (9.8 g, 40 mmol), triethylamine (33 mL, 240 mmol), and ammonium chloride (11 g, 200 mmol) in DMF (40 mL) was added PyBOP (21.9 g, 42 mmol) in five portions. The reaction was complete in 2 h, as determined by LCMS analysis. The reaction mixture was poured into water (1.5 L) and stirred for 10 minutes. The precipitate was collected by filtration and dried overnight under high vacuum to give 6-(2-methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxamide. 1H NMR (300 MHz, CDCl3) δ 8.40 (s, 0.7H), 8.05 (m, 1.3H), 7.74 (bs, 1H), 7.44 (m, 1H), 7.05 (m, 2H), 5.78 (bs, 1H), 3.92 (s, 3H); 2.65 (s, 3H). HPLC ret. time 2.71 min, 10-100% CH3CN, 5 min gradient; ESI-MS m/z 245.9 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822451B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-de42c27c4d3f4307a5aa952636231542
출처 메모uspto-grants-2014_09