Hydrochloric Acid → HCID 19599415, compound
Reaction equation
[CH:1]1[CH:9]=[CH:8][CH:7]=[C:6]2[C:2]=1[C:3]([C:15]([O:17]CC)=[O:16])=[C:4]1[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][N:5]12.[OH-].[Na+].Cl>>[CH:1]1[CH:9]=[CH:8][CH:7]=[C:6]2[C:2]=1[C:3]([C:15]([OH:17])=[O:16])=[C:4]1[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][N:5]12Participants
4
Procedure
The title compound (D5) was prepared from ethyl 7,8,9,10-tetrahydro-6H-azepino[1,2-a]indole-11-carboxylate by hydrolysis with sodium hydroxide as in the method of Description 3d. After 4 hours heating under reflux, the mixture was acidified with 5M HCl acid and the white solid formed filtered off and dried (82%).
Workup
- temperatureAfter 4 hours heating
- temperatureunder reflux
- customthe white solid formed
- filtrationfiltered off
- customdried (82%)
Sources & evidence
- ORD record
- ord-9f4d0b4e65174d1199fe3f3648fb6036
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998409
Reaction notes
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