戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 252978作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-DimethylaminopyridineHCID 21885—
反応物3-Methoxyphenyl isocyanateHCID 87843—
反応物3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propan-1-olHCID 66840679—
溶媒AcetonitrileHCID 6342—
生成物(3-methoxy-phenyl)-carbamic acid 3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl esterHCID 66841255—

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872005B2
出典データセットuspto-grants-2011_01
ORD IDord-82d6c132e0e44fc6b47f970f7b5632cb
出典メモuspto-grants-2011_01