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HRID 904607作成日:2026年10月24日

Phenacyl bromide → 6,6-Dimethyl-8-Keto-2-Phenyl-5,6,7,8-Tetrahydroimidazo[2,1-b]Benzothiazole

https://huagongshe.com/ja/reaction/904607

反応式

関与物質

役割名称HCID仕込み量
反応物Phenacyl bromideHCID 6259—
反応物2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-oneHCID 587874—
溶媒ChloroformHCID 6212—
生成物6,6-Dimethyl-8-Keto-2-Phenyl-5,6,7,8-Tetrahydroimidazo[2,1-b]BenzothiazoleHCID 914349—

反応手順

A 0.08 m. quantity each of 2-amino-5,5-dimethyl-7-keto-4,5,6,7-tetrahydrobenzothiazole and α-bromoacetophenone are mixed in 150 ml. of chloroform and heated at reflux for 4 hours. The slurry is filtered hot and the insoluble intermediate product is suspended in 600 ml. of water containing 25 g. of sodium acetate. This suspension is heated slowly to boil over 21/2 hours, then allowed to cool. The product is filtered off, washed well with water and dried yielding 12.5 g. of product melting at 175°-178° C. and having the structure: ##STR9##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04419289
出典データセットuspto-grants-1983_12
ORD IDord-4aeffa7437c3443e9edad411b9b5c150
出典メモuspto-grants-1983_12