Hydrochloric Acid → HCID 178464133, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1([OH:38])[C:17]2[C:12](=[CH:13][C:14]([C:22]3[O:23][CH:24]=[CH:25][N:26]=3)=[CH:15][C:16]=2[C:18]([F:21])([F:20])[F:19])[N:11]([CH2:27][C@H:28]2[CH2:31][C@H:30]([N:32]([CH2:35][CH3:36])[CH2:33][CH3:34])[CH2:29]2)[C:10]1=[O:37].Cl>C(#N)C>[ClH:1].[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1([OH:38])[C:17]2[C:12](=[CH:13][C:14]([C:22]3[O:23][CH:24]=[CH:25][N:26]=3)=[CH:15][C:16]=2[C:18]([F:19])([F:20])[F:21])[N:11]([CH2:27][C@H:28]2[CH2:29][C@H:30]([N:32]([CH2:33][CH3:34])[CH2:35][CH3:36])[CH2:31]2)[C:10]1=[O:37]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of the compound of Example 14-3 (80 mg, 0.140 mmol) in acetonitrile (1 mL) was added 4N hydrochloric acid (0.1 mL), and the mixture was concentrated in vacuo and dried to give the titled compound (80 mg, quant.).
Workup
- concentrationthe mixture was concentrated in vacuo
- customdried
Sources & evidence
- ORD record
- ord-f025825f6f4f4d66aac312950252652c
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825155B2
Reaction notes
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