戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 280373作成日:2026年10月27日

Phenol → (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic Acid Phenyl Ester

https://huagongshe.com/reaction/280373

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物TriethylamineHCID 8471—
反応物Sodium BicarbonateHCID 516892—
反応物N,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chlorideHCID 21249497—
反応物(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acidHCID 54200705—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic Acid Phenyl EsterHCID 54508713—

反応手順

A solution of 1.30 g (5 mmols) (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid, 1.27 g (5 mmols) N,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chloride, 0.49 g (5.2 mmols) phenol, and 1.10 g (10 mmols) triethylamine, in 10 ml dichloromethane was stirred at room temperature, under nitrogen atmosphere for 18 hours. Then, 10 ml of water (made slightly basic with sodium bicarbonate) were added. The precipitate was filtered of and the filtrate was dried over anhydrous magnesium sulfate, and evaporated to dryness under reduced pressure. The residual orange-yellow solid was recrystallized from anhydrous ethanol. Yield--0.62 g. Mp 194°-195° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04588812
出典データセットuspto-grants-1986_05
ORD IDord-9bc3fb30f72f49fa81b82afc6e70df78
出典メモuspto-grants-1986_05