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HRID 277119作成日:2026年10月26日

Sodium Hydroxide → methyl N'-[(Z)-[1-amino-2-(benzenesulfonyl)ethylidene]amino]carbamimidothioate

https://huagongshe.com/reaction/277119

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Sodium BicarbonateHCID 516892—
反応物Hydrazinecarboximidothioic acid methyl ester hydroiodideHCID 2774472—
反応物Sodium MethoxideHCID 10942334—
反応物2-(Phenylsulfonyl)-ethanimidic acid ethyl ester hydrochlorideHCID 70089441—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物methyl N'-[(Z)-[1-amino-2-(benzenesulfonyl)ethylidene]amino]carbamimidothioateHCID 17850406253%

反応手順

A suspension of 211 g (0.80 mol) 2-(phenylsulfonyl)-ethanimidic acid ethyl ester hydrochloride in 2 l chloroform was treated with 801 ml 1N aqueous sodium hydoxide. 350 ml of a saturated aqueous sodiumbicarbonate solution was added and the mixture was extracted with chloroform. The extracts were combined and dried with sodium sulfate and the solvents were distilled off under reduced pressure. The resulting oil was dissolved in 450 ml ethanol and the solution was added to a suspension of 44.6 g (0.82 mol) sodiummethylate and 187 g (0.80 mol) methyl aminomethanehydrazonothioate hydroiodide. After 75 minutes at room temperature 4.8 l of a 3/1 water/saturated aqueous sodiumbicarbonate solution was added and the mixture was extracted with chloroform. The organic phase was dried with sodiumsulfate and the solvents were evaporated. Recrystallisation from 1.81 ethanol gave 121 g (53%) 1-[[1-amino-2-(phenylsulfonyl)ethylidene]amino]-2-methyl-2-thiopseudourea (or tautomer), MS m/e (%): 287 (M+H+, 100), 270 (28).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355653B1
出典データセットuspto-grants-2002_03
ORD IDord-405a3525525f4c43958550aae1c8409e
出典メモuspto-grants-2002_03