Hydrochloric Acid → HCID 86615264, compound
Reaction equation
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][N:2]1[C:11]1[N:12]=[C:13]([CH:30]=[O:31])[CH:14]=[C:15]2[C:19]([CH3:20])=[C:18]([CH3:21])[N:17]([CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[C:25]([F:29])[CH:24]=3)[C:16]=12.[ClH:32]>C(OCC)(=O)C>[ClH:32].[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][N:2]1[C:11]1[N:12]=[C:13]([CH:30]=[O:31])[CH:14]=[C:15]2[C:19]([CH3:20])=[C:18]([CH3:21])[N:17]([CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[C:25]([F:29])[CH:24]=3)[C:16]=12Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 7-(3,4-dihydro-1H-isoquinolin-2-yl)-1-(3-fluorobenzyl)-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridin-5-carbaldehyde prepared in Step 1 in ethyl acetate was saturated with hydrochloric acid gas and then filtered to give 20 mg of the titled compound as a white solid.
Workup
- filtrationfiltered
Sources & evidence
- ORD record
- ord-3eaaed9e65714cb9b5937b4558119ed8
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662832B2
Reaction notes
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