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HRID 10946作成日:2026年10月23日

O-Phenylenediamine → Ethyl 3-{[(3'-{[(2-aminoanilino)carbothioyl]amino}[1,1'-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate

https://huagongshe.com/ja/reaction/10946

反応式

関与物質

役割名称HCID仕込み量
反応物O-PhenylenediamineHCID 7243—
反応物ThiophosgeneHCID 10040—
反応物Ethyl 3-{[(3'-amino[1,1'-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoateHCID 21982473—
溶媒TolueneHCID 1140—
溶媒Tetrahydrofuran tolueneHCID 22635083—
生成物Ethyl 3-{[(3'-{[(2-aminoanilino)carbothioyl]amino}[1,1'-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoateHCID 21982385—

反応手順

31.84 g (75 mmol) ethyl 3-{[(3′-amino[1,1′-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate 10.1.2 were dissolved in 600 ml toluene and 8.62 g thiophosgene were added. The mixture was refluxed for 2 h, evaporated and the residue dissolved in 200 ml toluene. This solution was added dropwise to a solution of o-phenylendiamine (12.2 g 113 mmol) in 500 ml tetrahydrofurane/toluene (1/1) at 40° C. The mixture was stirred for 12 h at room temperature, concentrated and purified (flash chromatography: dichloromethane/acetic acid ethyl ester 10+1) to yield 43 g (100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094911B2
出典データセットuspto-grants-2006_08
ORD IDord-796ff312c8e04ffba5526c15fe31e9ab
出典メモuspto-grants-2006_08