1,3-Diamino-2-propanol → HCID 18433113, 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]([Cl:18])=[C:14]([Cl:19])[CH:13]=2)[CH:3]=1.[NH2:20][CH2:21][CH:22]([OH:25])[CH2:23][NH2:24]>>[ClH:1].[NH2:20][CH2:21][CH:22]([OH:25])[CH2:23][NH:24][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]([Cl:18])=[C:14]([Cl:19])[CH:13]=2)[CH:3]=1Participants
3
Procedure
The title compound, m.p. 230-24° C., and MS: m/e=362.1 (M+H+), was prepared from 4-chloro-2-(3,4-dichloro-phenyl)-quinoline and 1,3-diamino-2-propanol.
Sources & evidence
- ORD record
- ord-2e1da5df2abe451e88569f066696dc29
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06440995B1
Reaction notes
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