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HRID 18679作成日:2026年10月23日

Ethanol → Ethyl 2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-6-carboxylate hydrobromide

https://huagongshe.com/ja/reaction/18679

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物BromineHCID 24408—
反応物Ethyl 4-oxocyclohexanecarboxylateHCID 317638—
反応物ThioureaHCID 2723790—
溶媒AcetoneHCID 180—
生成物Ethyl 2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-6-carboxylate hydrobromideHCID 8661435847.2%

反応条件

温度0 °C

反応手順

A 3 liter reactor equipped with mechanical stirrer, thermometer and condenser was loaded with 1500 ml of ethanol and 200 g of 4-oxo-cyclohexanecarboxylic acid ethyl ester. After cooling to 0° C., 188 g of bromine were dropped therein in about 1 hour. The temperature was raised to 10° C., then to the room one after discolouration. After 1 hour, 89.32 g of thiourea were added in portions to obtain a suspension, that was refluxed to obtain gradual dissolution of the solid. After 4 hours the solution was concentrated to small volume to obtain a solid mass, that was suspended in 800 ml of acetone and refluxed to obtain a solution. The solution was then cooled to room temperature to precipitate a solid, then to 0° C. and after 4 hours the solid was filtered, washed twice with 100 ml of cold acetone and dried to obtain 170 g of the title product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741490B2
出典データセットuspto-grants-2010_06
ORD IDord-36d9fa800331458bb2edcf0bb26dcc5f
出典メモuspto-grants-2010_06