反応式
CN(C=[N:5][S:6]([C:9]1[C:10]([C:15]2[CH:20]=[CH:19][C:18]([CH2:21][N:22]3[C:26]([C:27]4[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=4)=[C:25]([C:33]4[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=4)[N:24]=[C:23]3[C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)=[CH:17][CH:16]=2)=[CH:11][CH:12]=[CH:13][CH:14]=1)(=[O:8])=[O:7])C>C(O)C.Cl>[C:39]1([C:23]2[N:22]([CH2:21][C:18]3[CH:17]=[CH:16][C:15]([C:10]4[C:9]([S:6]([NH2:5])(=[O:8])=[O:7])=[CH:14][CH:13]=[CH:12][CH:11]=4)=[CH:20][CH:19]=3)[C:26]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)=[C:25]([C:33]3[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=3)[N:24]=2)[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1参加物
4
実験手順
1.9 g of 4′-(2,4,5-triphenylimidazol-1-ylmethyl)biphenyl-2-sulfonic acid dimethylaminomethylenamide in 20 ml of ethanol and 20 ml of a saturated aqueous HCl solution are refluxed for 3 h. The volatile constituents are removed in vacuo, the residue is stirred with 100 ml of water and the product is filtered off. 1.0 g of an amorphous powder is obtained.
後処理
- customThe volatile constituents are removed in vacuo
- filtrationthe product is filtered off
出典と根拠
- ORDレコード
- ord-2819804ff7e8469ab870846ac50f3c59
- 出典データセット
- uspto-grants-2002_11
- 特許番号
- US06486189B2
関連ノート
読み込み中…