3-Amino-1,2-propanediol → HCID 18432996, compound
Reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[C:14]([CH3:20])[CH:13]=2)[CH:3]=1.[NH2:21][CH2:22][CH:23]([OH:26])[CH2:24][OH:25]>>[ClH:1].[CH3:19][O:18][C:15]1[CH:16]=[CH:17][C:12]([C:4]2[CH:3]=[C:2]([NH:21][CH2:22][CH:23]([OH:26])[CH2:24][OH:25])[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[N:5]=2)=[CH:13][C:14]=1[CH3:20]Participants
3
Procedure
The title compound, m.p. 166-171° C., and MS: m/e=338 (M+), was prepared from 4-chloro-2-(4-methoxy-3-methyl-phenyl)-quinoline and (RS)-3-amino-1,2-propandiol.
Sources & evidence
- ORD record
- ord-3a22bf7b3f8b4cae912062a367d13a6d
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06440995B1
Reaction notes
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