돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1356071생성일: 2026년 10월 26일

Sodium Carbonate → 2-Amino-4-(4-methyl-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/1356071

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Amino-4-chloro-6-methylsulfanyl-pyrimidine-5-carbonitrileHCID 18507260—
반응물2-(4-Methyl-furan-2-yl)-benzo[1,3,2]dioxaboroleHCID 18507588—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매BenzeneHCID 241—
생성물2-Amino-4-(4-methyl-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrileHCID 1850749147%

반응 조건

온도90 °C

반응 단계

To a stirred suspension of 2.19 g (10.9 mmol) 2-amino-4-chloro-6-methylsulfanyl-pyrimidine-5-carbonitrile in 40 ml benzene at room temperature were added 2,40 g (12.0 mmol) 2-(4-methyl-furan-2-yl)-benzo[1,3,2]dioxaborole, 252mg (0.22 mmol) tetrakis(triphenylphosphine)palladium(O) and 11 ml (22.0 mmol) 2M aqueous sodium carbonate. The reaction mixture was heated at 90° C. for 16 h, then concentrated in vacuo. Chromatography (1/3 ethyl acetate/hexane then 1/1 ethyl acetate/hexane) afforded 1.26 g (47%) 2-amino-4-(4-methyl-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile as a light yellow crystalline solid. EI-MS m/e (%): 246 (M+, 61), 245 ([M—H]+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06586441B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-b629dd33f06e4fe5846ff2e1d6e33a8f
출처 메모uspto-grants-2003_07