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HRID 68936作成日:2026年10月25日

2-Amino-4,5,6,7-tetrahydrobenzothiazole → 2-methylsulfanyl-4-oxo-5,6,7,8-tetrahydro-4H-9-thia-1,4a-diaza-fluorene-3-carboxylic acid

https://huagongshe.com/reaction/68936

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4,5,6,7-tetrahydrobenzothiazoleHCID 18046—
反応物5-[Bis(ethylsulfanyl)methylidene]-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 13679812—
溶媒EthanolHCID 702—
生成物2-methylsulfanyl-4-oxo-5,6,7,8-tetrahydro-4H-9-thia-1,4a-diaza-fluorene-3-carboxylic acidHCID 6711710746.8%

反応条件

温度87.5 °C

反応手順

The suspension of 4,5,6,7-tetrahydro-benzothiazol-2-yl-amine (8 gm, 0.0519 mol) and 5-(bis-ethylsulfanyl-methylene)-2,2-dimethyl-[1,3]dioxane-4,6-dione (14.2 gm, 0.0572 mol) in ethanol (60 ml) was heated at 85-90° C. for 10 hours. Reaction mixture was cooled to room temperature and filtered. The solid, thus obtained, was washed with ethanol (20 ml) followed by with diethyl ether (50 ml) and suck dried to give 7.2 gm of title compound as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822484B2
出典データセットuspto-grants-2014_09
ORD IDord-1d8e0f44e55846caa74804a84a556536
出典メモuspto-grants-2014_09