Ethanolamine → HCID 18433062, 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:21]=[CH:20][C:19]3[CH2:18][CH2:17][CH2:16][CH2:15][C:14]=3[CH:13]=2)[CH:3]=1.[CH2:22]([CH2:24][NH2:25])[OH:23]>>[ClH:1].[CH:13]1[C:14]2[CH2:15][CH2:16][CH2:17][CH2:18][C:19]=2[CH:20]=[CH:21][C:12]=1[C:4]1[CH:3]=[C:2]([NH:25][CH2:24][CH2:22][OH:23])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=1Participants
3
Procedure
The title compound, m.p. 250-252° C. and MS: m/e=319.4 (M+H+), was prepared from 4-chloro-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-quinoline and ethanolamine.
Sources & evidence
- ORD record
- ord-57b5849410d24aa5966c8be1a320cd3d
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06440995B1
Reaction notes
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