돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434647생성일: 2026년 10월 26일

Sodium Carbonate → 5-Chloro-1-(2-triphenylmethylaminothiazol-4-ylmethyl)pyrimidin-2-one

https://huagongshe.com/reaction/434647

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물5-Chloro-2(1H)-pyrimidinoneHCID 108578—
반응물4-Chloromethyl-2-tritylaminothiazoleHCID 13745172—
촉매Benzyltrimethylammonium chlorideHCID 5963—
용매DimethylformamideHCID 6228—
생성물5-Chloro-1-(2-triphenylmethylaminothiazol-4-ylmethyl)pyrimidin-2-oneHCID 2049177379.4%

반응 조건

온도90 °C

반응 단계

A stirred suspension of 5-chloropyrimidin-2-one (688 mg), 4-chloromethyl-2-triphenylmethylaminothiazole (3.000 g), anhydrous sodium carbonate (1.086 g) and benzyltrimethylammonium chloride (20 mg) in dry N,N-dimethylformamide (25 ml) was heated at 90° C. After 1.5 h the reaction mixture was evaporated to dryness. The residue was suspended in ethyl acetate (250 ml) and washed with water (2×60 ml) and brine (60 ml), then dried and evaporated to a dark brown foam. The foam was subjected to column chromatography on silica developing and eluting with chloroform-ethanol, 24:1. This gave a brown foam which was triturated with diethyl ether to give a brown solid (2.03 g). A portion of the solid (360 mg) was recrystallised from ethyl acetate to give buff crystals of the title pyrimidinone (129 mg), m.p. 215°-216° C., λmax (EtOH) 268 nm (ε 8,630), 335 nm (ε 3,440).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04399140
출처 데이터셋uspto-grants-1983_08
ORD IDord-a2a003919abc43a1bab526a3d49447b9
출처 메모uspto-grants-1983_08