Hydrochloric Acid → HCID 67142381, compound
Reaction equation
[CH3:1][C:2]1[NH:20][C:5]2=[C:6]([N:10]3[CH2:19][CH2:18][C:17]4[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=4)[CH2:11]3)[N:7]=[CH:8][CH:9]=[C:4]2[C:3]=1[S:21][CH3:22].[ClH:23]>C(OCC)(=O)C>[ClH:23].[CH3:1][C:2]1[NH:20][C:5]2=[C:6]([N:10]3[CH2:19][CH2:18][C:17]4[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=4)[CH2:11]3)[N:7]=[CH:8][CH:9]=[C:4]2[C:3]=1[S:21][CH3:22]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-(2-methyl-3-methylsulfanyl-1H-pyrrolo[2,3-c]pyridin-7-yl)-1,2,3,4-tetrahydroisoquinoline prepared in Step 2 in ethyl acetate was saturated with hydrochloric acid gas and then filtered to give the titled compound as a white solid (Yield: 54%)
Workup
- filtrationfiltered
Sources & evidence
- ORD record
- ord-651464023cd645e6ac3783a9141c38b6
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662832B2
Reaction notes
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