Hydrogen chloride-ethyl acetate → HCID 67360608, compound
Reaction equation
C(OCC)(=O)C.[ClH:7].[Cl:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[S:23][C:22]3[C:21](=[O:24])[N:20]([CH2:25][CH2:26][C:27]4[CH:47]=[CH:46][C:30]([CH2:31][N:32]5[CH2:37][CH2:36][N:35](C(OC(C)(C)C)=O)[CH2:34][C:33]5=[O:45])=[CH:29][CH:28]=4)[CH:19]=[N:18][C:17]=3[CH:16]=2)=[CH:11][CH:10]=1>>[ClH:8].[ClH:7].[Cl:8][C:9]1[CH:10]=[CH:11][C:12]([C:15]2[S:23][C:22]3[C:21](=[O:24])[N:20]([CH2:25][CH2:26][C:27]4[CH:28]=[CH:29][C:30]([CH2:31][N:32]5[CH2:37][CH2:36][NH:35][CH2:34][C:33]5=[O:45])=[CH:46][CH:47]=4)[CH:19]=[N:18][C:17]=3[CH:16]=2)=[CH:13][CH:14]=1Participants
3
Procedure
4N Hydrogen chloride-ethyl acetate solution (6 ml) was added to the compound (75 mg) obtained in Example 37, and the mixture was stirred at room temperature for 1 hr. The solvent was evaporated under reduced pressure, and the residue was washed with ethyl acetate to give the title compound (72 mg) as a colorless powder.
Workup
- customThe solvent was evaporated under reduced pressure
- washthe residue was washed with ethyl acetate
Sources & evidence
- ORD record
- ord-c92b98bbd2c84be1a80054b114e14776
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07989445B2
Reaction notes
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