Morpholine → HCID 71075085、化合物

HRID 2170713ノート

反応式

HRID 2170713 の反応式
[CH3:1][O:2][C:3](=[O:32])[C@@H:4]([O:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]([N:15]2[C:23]3[C:18](=[CH:19][C:20]([C:24]([O:26]CC=C)=[O:25])=[CH:21][CH:22]=3)[C:17]([CH3:30])=[C:16]2[CH3:31])[CH3:14])=[CH:9][CH:8]=1)[CH3:5].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>[CH3:1][O:2][C:3](=[O:32])[C@@H:4]([O:6][C:7]1[CH:8]=[CH:9][C:10]([CH:13]([N:15]2[C:23]3[C:18](=[CH:19][C:20]([C:24]([OH:26])=[O:25])=[CH:21][CH:22]=3)[C:17]([CH3:30])=[C:16]2[CH3:31])[CH3:14])=[CH:11][CH:12]=1)[CH3:5]

参加物

5

実験手順

The mixture of allyl 1-(1-(4-(((S)-1-methoxy-1-oxopropan-2-yl)oxy)phenyl)ethyl)-2,3-dimethyl-1H-indole-5-carboxylate (0.55 g, 1.26 mmol) and morpholine (1.0 mL, 12.6 mmol) in THF (5 mL) was degassed and then Pd(PPh3)4 (0.15 g, 0.13 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 pH 4. The solvent was removed and the residue was purified by silica gel chromatography to obtain the title compound. ESI-MS (m/z): 396 [M+H]+.

後処理

  1. customwas degassed
  2. customThe solvent was removed
  3. dissolutionthe residue was dissolved in Methanol
  4. customThe solvent was removed
  5. customthe residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-0a2be60e77af4bcbbf9eff1dbb57654a
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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