1,4-Dioxane hydrochloride → (R)-1-(4-trifluoromethyl-benzenesulfonyl)-piperazine-2-carboxylic acid 3-fluoro-4-trifluoromethoxy-benzylamide hydrochloride
反応式
C(OC([N:8]1[CH2:13][CH2:12][N:11]([S:14]([C:17]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][CH:18]=2)(=[O:16])=[O:15])[C@@H:10]([C:27](=[O:42])[NH:28][CH2:29][C:30]2[CH:35]=[CH:34][C:33]([O:36][C:37]([F:40])([F:39])[F:38])=[C:32]([F:41])[CH:31]=2)[CH2:9]1)=O)(C)(C)C.[ClH:43].O1CCOCC1>O1CCOCC1>[ClH:43].[F:41][C:32]1[CH:31]=[C:30]([CH:35]=[CH:34][C:33]=1[O:36][C:37]([F:40])([F:38])[F:39])[CH2:29][NH:28][C:27]([C@H:10]1[CH2:9][NH:8][CH2:13][CH2:12][N:11]1[S:14]([C:17]1[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][CH:18]=1)(=[O:15])=[O:16])=[O:42]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of the compound (60 mg) obtained in Step 4 in 1,4-dioxane (0.6 ml) was added 4N hydrogen chloride/1,4-dioxane solution (0.6 ml) with stirring at room temperature. After stirring at room temperature for 2 days, the reaction mixture was concentrated under reduced pressure. Toluene was added to the residue, and the mixture was concentrated again under reduced pressure to give a crude product (about 0.095 mmol) containing the title compound as a main component. The obtained crude product was directly used for the next reaction.
後処理
- stirringAfter stirring at room temperature for 2 days
- concentrationthe reaction mixture was concentrated under reduced pressure
- additionToluene was added to the residue
- concentrationthe mixture was concentrated again under reduced pressure
- customto give a crude product (about 0.095 mmol)
出典と根拠
- ORDレコード
- ord-3d49b9b5b47c4948876f19314de3dd18
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08017612B2
反応ノート
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