HCID 19895770, compound → HCID 19895762, compound
Reaction equation
[CH2:1]([N:4]([CH:18]1[CH2:27][CH2:26][C:25]2[C:20](=[CH:21][CH:22]=[CH:23][C:24]=2[OH:28])[CH2:19]1)[CH2:5][CH2:6][N:7]1[C:15](=O)[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8]1=O)[CH2:2][CH3:3].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH2:8]1[C:9]2[C:14](=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:15][N:7]1[CH2:6][CH2:5][N:4]([CH2:1][CH2:2][CH3:3])[CH:18]1[CH2:27][CH2:26][C:25]2[C:24]([OH:28])=[CH:23][CH:22]=[CH:21][C:20]=2[CH2:19]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product of Example 13 was reduced with LAH in dry THF and, after purification, the isolated compound was characterized by its HCl.salt NMR, (CD3OD) δ7.7 (m, 4H), 6.9 (m, 1H), 6.6 (m, 2H), 1.0 (t, 3H).
Workup
- customafter purification
Sources & evidence
- ORD record
- ord-76c1cb9457da4529824b74fee485dd75
- Source dataset
- uspto-grants-1992_06
- Patent number
- US05118704
Reaction notes
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