돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325802생성일: 2026년 10월 25일

Octane → N-(5-Methyl-2-propargyloxyphenylsulfonyl)-N'-(4-chloro-6-methoxypyrimidin-2-yl)-urea

https://huagongshe.com/reaction/325802

반응식

참여 물질

역할이름HCID투입량
반응물OctaneHCID 356—
반응물2-Pyrimidinamine, 4-chloro-6-methoxy-HCID 79811—
반응물5-Methyl-2-propargyloxyphenylsulfonylisocyanateHCID 13472953—
용매TetrahydrofuranHCID 8028—
생성물N-(5-Methyl-2-propargyloxyphenylsulfonyl)-N'-(4-chloro-6-methoxypyrimidin-2-yl)-ureaHCID 13472954—

반응 단계

A solution of 9.4 g of crude 5-methyl-2-propargyloxyphenylsulfonylisocyanate in 50 ml of absolute tetrahydrofuran is added dropwise at room temperature, within 10 minutes, to a solution of 3.7 g of 2-amino-4-chloro-6-methoxy-pyrimidine and 0.1 g of 1,4-diazadicyclo[2.2.2]octane in 60 ml of absolute tetrahydrofuran, in the course of which the temperature rises slightly. The reaction solution is stirred for 18 hours at room temperature; it is then filtered, and concentrated by evaporation. The residue is crystallised from ethyl acetate to thus obtain 5.8 g of N-(5-methyl-2-propargyloxyphenylsulfonyl)-N'-(4-chloro-6-methoxy-pyrimidin-2-yl)-urea, m.p. 202°-204° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04443243
출처 데이터셋uspto-grants-1984_04
ORD IDord-d1f601befbce40ebb817445180d90ed2
출처 메모uspto-grants-1984_04