Hydrochloric Acid → HCID 54144080, compound
Reaction equation
[OH:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[CH:4]=[CH:5][C:6]1[CH:15]=[CH:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]=1.[CH3:20][N:21]([CH2:23][CH2:24]Cl)[CH3:22].Cl>>[CH3:20][N:21]([CH3:22])[CH2:23][CH2:24][O:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[CH:4]=[CH:5][C:6]1[CH:15]=[CH:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]=1Participants
4
Procedure
2-[o-(β-Dimethylamino-ethoxy)-styryl]-quinoline was prepared from 2-(o-hydroxy-styryl)-quinoline (m.p. 274°-278° C.) and dimethylamino-ethyl chloride, and the free base was converted into its monohydrochloride, yielding 86% of theory of the compound of the formula ##STR8## which had a melting point of 188° C.
Workup
- customyielding 86% of theory of the compound of the formula ##STR8## which
Sources & evidence
- ORD record
- ord-138592e6f6b94b03a62624ce5a227f36
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04130650
Reaction notes
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