Morpholine → HCID 71075610、化合物
反応式
[C:1]([C:3]([C:6]1[CH:7]=[C:8]([CH:27]=[CH:28][CH:29]=1)[CH2:9][N:10]1[C:18]2[C:13](=[CH:14][C:15]([C:19]([O:21]CC=C)=[O:20])=[CH:16][CH:17]=2)[C:12]([CH3:25])=[C:11]1[CH3:26])([CH3:5])[CH3:4])#[N:2].N1CCOCC1>C1COCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:1]([C:3]([C:6]1[CH:7]=[C:8]([CH:27]=[CH:28][CH:29]=1)[CH2:9][N:10]1[C:18]2[C:13](=[CH:14][C:15]([C:19]([OH:21])=[O:20])=[CH:16][CH:17]=2)[C:12]([CH3:25])=[C:11]1[CH3:26])([CH3:5])[CH3:4])#[N:2]参加物
5
実験手順
The mixture of allyl 1-(3-(2-cyanopropan-2-yl)benzyl)-2,3-dimethyl-1H-indole-5-carboxylate (0.688 g, 1.78 mmol) and morpholine (1.6 mL, 17.8 mmol) in THF (5 mL) was degassed and then Pd(PPh3)4 (0.21 g, 0.18 mmol) was added. The mixture was stirred at room temperature for 1 h. The solvent was removed and the residue was dissolved in Methanol and acidified to pH4. The solvent was removed and the residue was purified by silica gel to obtain the title compound. ESI-MS (m/z): 347 [M+H]+.
後処理
- customwas degassed
- customThe solvent was removed
- dissolutionthe residue was dissolved in Methanol
- customThe solvent was removed
- customthe residue was purified by silica gel
出典と根拠
- ORDレコード
- ord-44b3877c85414afba2a9b233191fd665
- 出典データセット
- uspto-grants-2015_06
- 特許番号
- US09051265B2
反応ノート
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