HCID 20029306, compound → HCID 20029320, compound
Reaction equation
[ClH:1].[C:2]([O:5][CH:6]([CH2:27][NH:28]C)[CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])(=[O:4])[CH3:3]>CCCCCC>[ClH:1].[C:2]([O:5][CH:6]([CH2:27][NH2:28])[CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])(=[O:4])[CH3:3]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2 a) (±)-3-methylamino-1-octadecyloxy-2-propyl acetate hydrochloride; m.p. 109°-113° C. from n-hexane; yield 61%.
Sources & evidence
- ORD record
- ord-7bd2622de33544ec8884061eb3ae0940
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04855489
Reaction notes
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