Hydrochloric Acid → HCID 68648873, compound
Reaction equation
C(O[C:6]([N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[C:11]([C:18]([O:20][CH3:21])=[O:19])[CH:12]=[CH:13][CH:14]=2)[CH2:9]1)=O)CCC.Cl>>[CH3:6][N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[C:11]([C:18]([O:20][CH3:21])=[O:19])[CH:12]=[CH:13][CH:14]=2)[CH2:9]1Participants
3
Procedure
2-butoxycarbonyl-1,2,3,4-tetrahydro-8-methoxycarbonyl-isoquinoline is deprotected with methanolic HCl and then methylated according to Example 11b.
Sources & evidence
- ORD record
- ord-6f3144b3a33d4493bfbae6f21f8359ee
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07807693B2
Reaction notes
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