Hydrochloric Acid → 11-Methyl-2,3,4,5-tetrahydro-1H-azepino[4,3-b]quinolin-5-ol--hydrogen chloride (1/2)
Reaction equation
C(OC([N:6]1[CH2:21][CH2:20][CH:19]([O:22]C(OCC)=O)[C:9]2=[N:10][C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:16]=3[C:17]([CH3:18])=[C:8]2[CH2:7]1)=O)C.[ClH:28]>>[ClH:28].[ClH:28].[OH:22][CH:19]1[C:9]2=[N:10][C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:16]=3[C:17]([CH3:18])=[C:8]2[CH2:7][NH:6][CH2:21][CH2:20]1Participants
3
Procedure
2,3,4,5-Tetrahydro-5-hydroxy-11-methyl-1H-azepino[4,3-b]quinoline dihydrochloride was prepared from 5-(ethoxy-carbonyloxy)-2,3,4,5-tetrahydro-11-methyl-1H-2-azepino[4,3-b]quinoline-carboxylic acid ethyl ester by hydrolysis with 2 N hydrochloric acid.
Sources & evidence
- ORD record
- ord-0ac794b1f1b84c0ab36193348fd8312d
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03987047
Reaction notes
Loading…