Phenylacetaldehyde → HCID 67706409, compound
Reaction equation
[ClH:1].Cl.[CH3:3][O:4][C:5](=[O:22])[CH2:6][CH2:7][NH:8][CH:9]1[CH2:14][CH2:13][N:12]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH2:11][CH2:10]1.[C:23]1([CH2:29][CH:30]=O)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.C([BH3-])#N.[Na+]>>[ClH:1].[ClH:1].[CH3:3][O:4][C:5](=[O:22])[CH2:6][CH2:7][N:8]([CH:9]1[CH2:10][CH2:11][N:12]([CH2:15][C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:13][CH2:14]1)[CH2:30][CH2:29][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1Participants
4
Procedure
Prepared from N-[1-benzyl-4-piperidinyl]-β-alanine methyl ester dihydrochloride, phenylacetaldehyde and sodium cyanoborohydride.
Sources & evidence
- ORD record
- ord-ce792801d4b142788ad8c74aeb3f7e58
- Source dataset
- uspto-grants-1997_12
- Patent number
- US05700801
Reaction notes
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