Hydrochloride methanol → Hydrochloric Acid
Reaction equation
C(O[C:6]([N:8]([CH:10]1[CH2:14][CH2:13][N:12]([S:15]([C:18]2[C:19]3[C:20]([Br:28])=[CH:21][N:22]=[CH:23][C:24]=3[CH:25]=[CH:26][CH:27]=2)(=[O:17])=[O:16])[CH2:11]1)C)=O)(C)(C)C.[ClH:29].CO>>[Br:28][C:20]1[C:19]2[C:18]([S:15]([N:12]3[CH2:13][CH2:14][CH:10]([NH:8][CH3:6])[CH2:11]3)(=[O:16])=[O:17])=[CH:27][CH:26]=[CH:25][C:24]=2[CH:23]=[N:22][CH:21]=1.[ClH:29]Participants
4
Procedure
Intermediate 20 (0.157 g) prepared in Step A mentioned above is added with 10% hydrogen chloride/methanol (2 ml), and the mixture is stirred at room temperature for 12 hours. The solvent is evaporated under reduced pressure to obtain the title compound as hydrochloride (125 mg (predictive yield)).
Workup
- customThe solvent is evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-dc3c812f30fd41919d23750e65b4bbc1
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07618984B2
Reaction notes
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