反応式
[OH:1][CH2:2][CH2:3][C:4]1[C:5]([C:25]([F:28])([F:27])[F:26])=[N:6][N:7]([CH2:9][C:10]([NH:12][C:13]2[S:17][C:16]3[CH2:18][CH2:19][CH2:20][CH2:21][C:15]=3[C:14]=2[C:22]([NH2:24])=[O:23])=[O:11])[CH:8]=1.C(N(CC)CC)C.[CH3:36][S:37](Cl)(=[O:39])=[O:38].O>C(Cl)Cl>[CH3:36][S:37]([O:1][CH2:2][CH2:3][C:4]1[C:5]([C:25]([F:26])([F:28])[F:27])=[N:6][N:7]([CH2:9][C:10]([NH:12][C:13]2[S:17][C:16]3[CH2:18][CH2:19][CH2:20][CH2:21][C:15]=3[C:14]=2[C:22](=[O:23])[NH2:24])=[O:11])[CH:8]=1)(=[O:39])=[O:38]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
2-(2-(4-(2-Hydroxyethyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide (Example 64, 480 mg, 1.153 mmol) was dissolved in DCM (10 mL). Triethylamine (117 mg, 1.153 mmol) was added, followed by methanesulfonyl chloride (132 mg, 1.153 mmol). The reaction mixture was stirred at RT for 3 h. Water was added and the reaction mixture extracted with DCM (×3). The combined DCM layers were then washed with brine, dried over MgSO4, filtered and the solvent removed in vacuo to yield the desired product (450 mg, 0.91 mmol, 79%).
後処理
- extractionthe reaction mixture extracted with DCM (×3)
- washThe combined DCM layers were then washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customthe solvent removed in vacuo
出典と根拠
- ORDレコード
- ord-e4f6d115e4d646668db695925a99d421
- 出典データセット
- uspto-grants-2010_10
- 特許番号
- US07820707B2
関連ノート
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