1,3-Diamino-2-propanol → HCID 18432962, 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]([CH3:18])=[CH:14][CH:13]=2)[CH:3]=1.[NH2:19][CH2:20][CH:21]([OH:24])[CH2:22][NH2:23]>>[ClH:1].[NH2:19][CH2:20][CH:21]([OH:24])[CH2:22][NH:23][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]([CH3:18])=[CH:14][CH:13]=2)[CH:3]=1Participants
3
Procedure
The title compound, m.p. 264-272° C. and MS: m/e=308.3 (M+H+), was prepared from 4-chloro-2-p-tolyl-quinoline and 1,3-diamino-2-propanol.
Sources & evidence
- ORD record
- ord-d54a890a28a74f56acb004b852c72568
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06440995B1
Reaction notes
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