Ethyl chloroformate → 3H-Azepino(4,5-b)quinoline-3-carboxylic acid, 1,2,4,5-tetrahydro-11-methyl-, ethyl ester
Reaction equation
C([N:3]1[CH2:17][CH2:16][C:15]2[C:6](=[N:7][C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:13]=3[C:14]=2[CH3:18])[CH2:5][CH2:4]1)C.Cl[C:20]([O:22][CH2:23][CH3:24])=[O:21]>>[CH2:23]([O:22][C:20]([N:3]1[CH2:17][CH2:16][C:15]2[C:6](=[N:7][C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:13]=3[C:14]=2[CH3:18])[CH2:5][CH2:4]1)=[O:21])[CH3:24]Participants
3
Procedure
1,2,4,5-Tetrahydro-11-methyl-3-azepino[4,5-b]quinoline-carboxylic acid ethyl ester was prepared from 3-ethyl-1,2,4,5-tetrahydro 11-methyl-3H-azepino[4,5-b]quinoline and ethyl chloroformate analogous to Example 59.
Sources & evidence
- ORD record
- ord-90bc7b0bd21a4f47ba4bced4da5e9cfc
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03987047
Reaction notes
Loading…