反応式
[C:1]([O:5][C:6](=[O:14])[C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1)([CH3:4])([CH3:3])[CH3:2].[C:15]([O:19][C:20](=[O:47])[CH:21]([NH:34][C:35](=[O:46])[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44]Br)[CH2:22][CH2:23][C:24]([O:26][CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[O:25])([CH3:18])([CH3:17])[CH3:16].C([O-])([O-])=O.[K+].[K+].N#N>C(#N)C>[C:15]([O:19][C:20](=[O:47])[CH:21]([NH:34][C:35](=[O:46])[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][O:13][C:10]1[CH:9]=[CH:8][C:7]([C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:14])=[CH:12][CH:11]=1)[CH2:22][CH2:23][C:24]([O:26][CH2:27][C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1)=[O:25])([CH3:16])([CH3:17])[CH3:18]参加物
6
実験手順
4-Hydroxy-benzoic acid tert-butyl ester (0.65 g, 3.08 mmol) was dissolved in acetonitrile (7.5 ml) and added to 2-(10-Bromodecanoylamino) pentanedioic acid 5-benzyl ester 1-tert-butyl ester (1.62 g, 3.08 mmol). Acetonitrile (90 ml) and K2CO3 (0.64 g, 4.62 mmol) was added and the mixture was refluxed for 16 h under a flow of N2. The solvent was removed under vacuum. AcOEt (100 ml) was added and the solution was washed with water (2×50 ml) using sat. NaCl and methanol to aid phase separation, dried over MgSO4, and concentrated to yield a light brown oil (2.18 g). The oil was purified by flash chromatography (silica, 95:5 DCM/AcOEt) to yield an oil (160 mg, 8%).
後処理
- customThe solvent was removed under vacuum
- additionAcOEt (100 ml) was added
- washthe solution was washed with water (2×50 ml)
- customphase separation
- dry with materialdried over MgSO4
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-685280ad0fbc4fcb9cd4dec5394b55cc
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08476228B2
関連ノート
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