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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252978생성일: 2026년 10월 26일

2-Dimethylaminopyridine → (3-methoxy-phenyl)-carbamic acid 3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl ester

https://huagongshe.com/reaction/252978

반응식

참여 물질

역할이름HCID투입량
반응물2-DimethylaminopyridineHCID 21885—
반응물3-Methoxyphenyl isocyanateHCID 87843—
반응물3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propan-1-olHCID 66840679—
용매AcetonitrileHCID 6342—
생성물(3-methoxy-phenyl)-carbamic acid 3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl esterHCID 66841255—

반응 조건

온도60 °C

반응 단계

S5; 3-{4-[N′-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propan-1-ol (355 mg, 1 mmol) was dissolved in acetonitrile (4 mL). To the mixture was added m-methoxyphenylisocyanate (149 mg., 1 mmol) and a catalytic amount of dimethylaminopyridine. The reaction was stirred at 60° C. for 16 hours. The reaction was then cooled to 4° C., and the precipitate was filtered, washed with acetonitrile (1 mL) and dried to give Compound 1, (3-methoxy-phenyl)-carbamic acid 3-{4-[N′-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872005B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-82d6c132e0e44fc6b47f970f7b5632cb
출처 메모uspto-grants-2011_01