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HRID 21729作成日:2026年10月25日

Sodium Hydroxide → 2,4-Dichloro-7-(6,6-dimethyl-3,5,6,7-tetrahydropyrrolo-[2,1-c][1,2,4]thiadiazol-3-ylidenamino)-6-fluorobenzothiazole

https://huagongshe.com/reaction/21729

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物BromineHCID 24408—
反応物2-Amino-4,4-dimethylpyrroline hydrochlorideHCID 19933461—
反応物2,4-Dichloro-6-fluoro-7-isothiocyanatobenzothiazoleHCID 19933464—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2,4-Dichloro-7-(6,6-dimethyl-3,5,6,7-tetrahydropyrrolo-[2,1-c][1,2,4]thiadiazol-3-ylidenamino)-6-fluorobenzothiazoleHCID 53968206—

反応条件

温度2 °C

反応手順

A solution of 2 g 2,4-dichloro-6-fluoro-7-isothiocyanatobenzothiazole in 10 ml dichloromethane was added, dropwise, at 0° C., to a suspension of 1.1 g 2-amino-4,4-dimethylpyrroline hydrochloride in 20 ml dichloromethane. A solution of 0.3 g sodium hydroxide and 6 ml water was added, dropwise, at 2° C. to this mixture which was stirred for 3 hours, whereby the temperature rose to 20° C. The mixture was cooled to -10° C. and a solution of 1 g bromine in 10 ml dichloromethane was added, dropwise, slowly and the mixture stirred for I hour whereby the temperature rose to 10° C. The solution was washed with water and with dilute caustic soda, dried over magnesium sulfate and concentrated. The residue was recrystallised from diisopropyl ether. Yield: 1.5 g=53% of theory m.p.: 134°-136° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424443
出典データセットuspto-grants-1995_06
ORD IDord-d804bd441201440e948ae6abc9e51e2d
出典メモuspto-grants-1995_06