돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2375298생성일: 2026년 10월 27일

Acetonitrile → 4-(1-Isopropyl-2-methylimidazol-5-yl)-2-[4-(3-morpholinopropylthio)anilino]pyrimidine

https://huagongshe.com/reaction/2375298

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물4-(1-Isopropyl-2-methylimidazol-5-yl)-2-[4-(3-hydroxypropylthio)anilino]pyrimidineHCID 69313108—
용매DichloromethaneHCID 6344—
생성물4-(1-Isopropyl-2-methylimidazol-5-yl)-2-[4-(3-morpholinopropylthio)anilino]pyrimidineHCID 6931061988%

반응 조건

온도80 °C

반응 단계

4-(1-Isopropyl-2-methylimidazol-5-yl)-2-[4-(3-hydroxypropylthio)anilino]pyrimidine (Method 84; 250 mg, 0.65 mmol) was suspended in DCM (8 ml) and acetonitrile (2 ml) and the stirred at room temperature under nitrogen. Triethylamine (100 μl) was added followed by dropwise addition of methane sulphonyl chloride (50 μl). The mixture was stirred for 2.5 hours and then allowed to stand for 18 hours. The volatiles were removed by evaporation, the residue dissolved in acetonitrile (5 ml), and morpholine (120 μl) and potassium carbonate (50 mg) were added. The mixture was stirred and heated at 80° C. for 3.5 hours and then the volatiles were removed by evaporation. The residue was partitioned between EtOAc (50 ml) and water (20 ml). The aqueous layer was basified to pH 9 with sodium bicarbonate solution. The phases separated and the aqueous layer re-extracted with EtOAc. The extracts were combined, washed with water (10 ml) and brine (10 ml), dried and then evaporated to give the title compound (260 mg, 88%) m/z 453.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07465728B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-aecfb62c33804ccfa2db9f65477ab6b7
출처 메모uspto-grants-2008_12