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Ethyl 3-{[(3'-{[(2-aminoanilino)carbothioyl]amino}[1,1'-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate → Ethyl 3-{[3'-(1H-benzimidazol-2-ylamino)[1,1'-biphenyl]3-yl]-sulfonylamino}-3-phenyl-propanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl 3-{[(3'-{[(2-aminoanilino)carbothioyl]amino}[1,1'-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate | HCID 21982385 | — |
| 触媒 | Mercuric oxide | HCID 30856 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Ethyl 3-{[3'-(1H-benzimidazol-2-ylamino)[1,1'-biphenyl]3-yl]-sulfonylamino}-3-phenyl-propanoate | HCID 21982519 | — |
反応手順
43 g (75 mmol) of Ethyl 3-{[(3′-{[(2-aminoanilino)carbothioyl]amino}[1,1′-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate 11.1.1 and 16.24 g (75 mmol) of yellow mercury oxide were mixed with 1.51 CHCl3 and refluxed for 6 h. The resulting material was purified via flash chromatography (dichloromethane/acetic acid ethyl ester 3+1). Recrystallization from acetic acid ethyl ester led to 27.8 g (68%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07094911B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-660d63e58a12491cb152bc9a8923af2b |
| 出典メモ | uspto-grants-2006_08 |