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HRID 65032作成日:2026年10月25日

Ethyl 3-chloro-3-oxopropionate → 2-Ethoxycarbonylacetylamino-4-(4-methoxyphenyl)-5-(3-pyridyl)-1,3-thiazole

https://huagongshe.com/reaction/65032

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 3-chloro-3-oxopropionateHCID 118931—
反応物2-Thiazolamine, 4-(4-methoxyphenyl)-5-(3-pyridinyl)-HCID 3024894—
反応物Sodium hydrochlorideHCID 23872008—
溶媒DimethylformamideHCID 6228—
生成物2-Ethoxycarbonylacetylamino-4-(4-methoxyphenyl)-5-(3-pyridyl)-1,3-thiazoleHCID 980094761%

反応手順

In 5 ml of dimethylformamide was dissolved 1 g of 2-amino-4-(4-methoxyphenyl)-5-(3-pyridyl)-1,3-thiazole. To the solution was added under ice-cooling 580 mg of ethoxycarbonylacetylchloride. The mixture was stirred for 30 minutes, to which was then added a saturated aqueous solution of sodium hydrogen chloride. The resultant was subjected to extraction with ethyl acetate. The organic layer was washed with water, dried and concentrated, followed by recrystallization from tetrahydrofuran to give 850 mg (61%) of 2-ethoxycarbonylacetylamino-4-(4-methoxyphenyl)-5-(3-pyridyl)-1,3-thiazole, m.p. 202°-203° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04612321
出典データセットuspto-grants-1986_09
ORD IDord-cc950e1f0a1b4feeaab27ac04899405e
出典メモuspto-grants-1986_09