反応式
[S:1](Cl)(=[O:4])(=[O:3])[NH2:2].C1(C)C=CC=CC=1.[OH:13][C:14]1[CH:19]=[CH:18][C:17]([CH:20]([N:28]([N:37]2[CH:41]=[N:40][N:39]=[CH:38]2)[C:29]2[CH:36]=[CH:35][C:32]([C:33]#[N:34])=[CH:31][CH:30]=2)[C:21]2[CH:26]=[CH:25][C:24]([OH:27])=[CH:23][CH:22]=2)=[CH:16][CH:15]=1>C(OCC)(=O)C.O.CN(C)C(=O)C>[S:1]([O:13][C:14]1[CH:19]=[CH:18][C:17]([CH:20]([N:28]([N:37]2[CH:41]=[N:40][N:39]=[CH:38]2)[C:29]2[CH:36]=[CH:35][C:32]([C:33]#[N:34])=[CH:31][CH:30]=2)[C:21]2[CH:26]=[CH:25][C:24]([O:27][S:1](=[O:4])(=[O:3])[NH2:2])=[CH:23][CH:22]=2)=[CH:16][CH:15]=1)(=[O:4])(=[O:3])[NH2:2]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 3
実験手順
Sulphamoyl chloride solution in toluene (5 mL, 0.7 M, 3.5 mmol) was concentrated under reduced pressure (30° C. water bath temperature) to ca. 1 mL volume. The residue was cooled to 0° C. (ice bath) and N,N-dimethylacetamide (5 mL) was added. 4-{[Bis-(4-hydroxy-phenyl)-methyl]-[1,2,4]triazol-4-yl-amino}-benzonitrile (CAB2070, 250 mg, 0.65 mmol) was added to the colourless solution and the mixture was stirred for 18 h at, room temperature. Ethyl acetate (50 mL) and water (30 mL) were added to the solution, the organic layer was separated, washed with water (2×30 mL) and brine (20 mL), dried over sodium sulphate and concentrated under reduced pressure to give a white solid. The solid was dissolved in ethyl acetate and precipitated by addition of hexane. The white powder was filtered off and dried under high vacuum. Yield: 299 mg (85%).
後処理
- additionwas added
- customthe organic layer was separated
- washwashed with water (2×30 mL) and brine (20 mL)
- dry with materialdried over sodium sulphate
- concentrationconcentrated under reduced pressure
- customto give a white solid
- customprecipitated by addition of hexane
- filtrationThe white powder was filtered off
- customdried under high vacuum
出典と根拠
- ORDレコード
- ord-3a71e3aaa6c843ed9a29a7fb1e9c4aea
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07745472B2
関連ノート
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