Ethanolamine → HCID 18433084, compound
Reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:12][CH3:13])=[CH:9][CH:10]=2)[N:5]=[C:4]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)[CH:3]=1.[CH2:21]([CH2:23][NH2:24])[OH:22]>>[ClH:1].[Cl:20][C:17]1[CH:18]=[CH:19][C:14]([C:4]2[CH:3]=[C:2]([NH:24][CH2:23][CH2:21][OH:22])[C:11]3[C:6](=[CH:7][C:8]([O:12][CH3:13])=[CH:9][CH:10]=3)[N:5]=2)=[CH:15][CH:16]=1Participants
3
Procedure
The title compound, m.p. 271-272° C., and MS: m/e=328 (M+), was prepared from 4-chloro-2-(4-chloro-phenyl)-7-methoxy-quinoline and ethanolamine.
Sources & evidence
- ORD record
- ord-8328a5624e064602bc031ecb5724f62a
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06440995B1
Reaction notes
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