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HRID 23357作成日:2026年10月25日

Cyclohexylthiourea → 7-[2-(Cyclohexylamino)-1,3-thiazol-5-yl]quinazolin-4(3h)-one

https://huagongshe.com/reaction/23357

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexylthioureaHCID 1471603—
反応物Bromo-(4-oxo-3,4-dihydro-quinazolin-7-yl)acetaldehydeHCID 135531132—
溶媒DimethylformamideHCID 6228—
生成物7-[2-(Cyclohexylamino)-1,3-thiazol-5-yl]quinazolin-4(3h)-oneHCID 135496165—

反応手順

A solution of bromo-(4-oxo-3,4-dihydro-quinazolin-7-yl)acetaldehyde and N-cyclohexylthiourea in dimethylformamide is heated at 70° C. until completion of the reaction (5-12 hours). The mixture is quenched with 10% dimethylamine in ethanol and the solvent is removed under reduced pressured. The crude is purified by chromatography on silica gel to isolate the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852720B2
出典データセットuspto-grants-2005_02
ORD IDord-25238562fd52496693cf85f9c426924f
出典メモuspto-grants-2005_02