Hydrochloric Acid → HCID 86611573, compound
Reaction equation
C([O:5][C:6](=[O:53])[CH:7]([N:11]([CH2:23][C:24]1[CH:29]=[CH:28][C:27]([C:30](=[O:52])[NH:31][CH2:32][CH2:33][O:34][CH2:35][CH2:36][O:37][CH2:38][CH2:39][O:40][CH2:41][CH2:42][NH:43][C:44](=[O:51])[CH2:45][CH2:46][CH2:47][C:48]([OH:50])=[O:49])=[CH:26][CH:25]=1)[S:12]([C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1)(=[O:14])=[O:13])[CH:8]([CH3:10])[CH3:9])(C)(C)C.Cl>ClCCl>[C:48]([CH2:47][CH2:46][CH2:45][C:44]([NH:43][CH2:42][CH2:41][O:40][CH2:39][CH2:38][O:37][CH2:36][CH2:35][O:34][CH2:33][CH2:32][NH:31][C:30]([C:27]1[CH:28]=[CH:29][C:24]([CH2:23][N:11]([S:12]([C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)(=[O:13])=[O:14])[CH:7]([CH:8]([CH3:10])[CH3:9])[C:6]([OH:53])=[O:5])=[CH:25][CH:26]=1)=[O:52])=[O:51])([OH:50])=[O:49]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Dichloromethane (5 ml) was added to the tert-butyl ester (Compound 14*; 50 mg, 0.046 mmol) and to the milky coloured solution which was obtained at ambient temperature was bobbled hydrochloric acid gas for 10 minutes. The mixture was evaporated to dryness and the residue was co-evaporated with dichloromethane (5×5 ml) to afford the product as white solid. Yield 47 mg (99%). M+1=1035.
Workup
- customwas obtained at ambient temperature
- customfor 10 minutes
- customThe mixture was evaporated to dryness
Sources & evidence
- ORD record
- ord-3790c3d11a3444f2a02b9d7af36130da
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08231858B2
Reaction notes
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