Hydrochloric Acid → HCID 67142041, compound
Reaction equation
[CH2:1]([N:8]1[C:12]2=[C:13]([NH:20][CH2:21][C:22]3[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=3)[N:14]=[C:15]([C:17]([OH:19])=[O:18])[CH:16]=[C:11]2[C:10]([CH3:29])=[C:9]1[CH3:30])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:31]>C(OCC)(=O)C>[ClH:31].[CH2:1]([N:8]1[C:12]2=[C:13]([NH:20][CH2:21][C:22]3[CH:23]=[CH:24][C:25]([F:28])=[CH:26][CH:27]=3)[N:14]=[C:15]([C:17]([OH:19])=[O:18])[CH:16]=[C:11]2[C:10]([CH3:29])=[C:9]1[CH3:30])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1-benzyl-7-(4-fluorobenzylamino)-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridin-5-carboxylic acid prepared in Step 1 in ethyl acetate was saturated with hydrochloric acid gas and then filtered to give 10.5 mg of the titled compound as a white solid.
Workup
- filtrationfiltered
Sources & evidence
- ORD record
- ord-a84bd136b49641819e2ecfbe840ea591
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662832B2
Reaction notes
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