HCID 18678498, compound → HCID 18678504, compound
Reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:14]1[CH2:19][CH2:18][CH:17]([C:20]([NH2:22])=O)[CH2:16][CH2:15]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>>[NH2:22][CH2:20][CH:17]1[CH2:16][CH2:15][N:14]([CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][OH:1])[CH2:19][CH2:18]1Participants
3
Procedure
Prepared from 1-(12-hydroxydodecyl)-piperidine-4-carboxamide (3.3 g, 10.6 mmol) and LAH (0.8 g, 21.2 mmol) according to general procedure used for Example 8 (Step B) to give 3.1 g of title compound as a white solid.
Sources & evidence
- ORD record
- ord-5c06f8f9714a40eebe598e37aa5a8a51
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506901B2
Reaction notes
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