Aluminium lithium hydride → HCID 22857203, compound
Reaction equation
[CH2:1]([N:3]1[C@@H:8]2[CH2:9][C:10]3[C:11]4[C:16]([NH:17][CH:18]=3)=[CH:15][CH:14]=[C:13]([O:19][CH3:20])[C:12]=4[C@@:7]2([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[O:6][CH2:5][C:4]1=O)[CH3:2].[H-].[H-].[H-].[H-].[Li+].[Al+3]>>[CH2:1]([N:3]1[C@@H:8]2[CH2:9][C:10]3[C:11]4[C:16]([NH:17][CH:18]=3)=[CH:15][CH:14]=[C:13]([O:19][CH3:20])[C:12]=4[C@@:7]2([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[O:6][CH:5]=[CH:4]1)[CH3:2]Participants
3
Procedure
Trans-7-ethyl-4,6,6a,8,9,10a-hexahydro-1-methoxy-10a-phenyl-7H-indolo[3,4-gh][1.4]benzoxazin-8-one (664 mg, 1.83 mmol) was reduced with LAH. The residue thus obtained was subjected to a silica gel column chromatography, eluting with n-hexane-ethyl acetate (3:1), to afford 74 mg (12%) of the title compound as a crude crystalline product (m.p.194-196 dec.)
Workup
- customThe residue thus obtained
- washeluting with n-hexane-ethyl acetate (3:1)
Sources & evidence
- ORD record
- ord-20a387e021e8472b80f47dca0b8f3046
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05466689
Reaction notes
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