Hydrochloric Acid → HCID 67773346, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:22]=[CH:21][C:6]([C:7]([N:9]([C@@H:11]([CH2:18][CH2:19][CH3:20])[CH2:12][N:13]2[CH2:16][CH:15]([OH:17])[CH2:14]2)[CH3:10])=[O:8])=[CH:5][CH:4]=1>CO>[ClH:2].[Cl:2][C:3]1[CH:4]=[CH:5][C:6]([C:7]([N:9]([C@@H:11]([CH2:18][CH2:19][CH3:20])[CH2:12][N:13]2[CH2:16][CH:15]([OH:17])[CH2:14]2)[CH3:10])=[O:8])=[CH:21][CH:22]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of hydrochloric acid in MeOH (0.1 M, 0.48 ml) was added (S)-4-Chloro-N-(1-(3-hydroxyazetidin-1-yl)pentan-2-yl)-N-methylbenzamide (Example 8.2A) (15 mg, 48 μmol) and allowed to evaporate. The product was dissolved in EtOAc (1 mL) and allowed to evaporate until dry.
Workup
- customto evaporate
- dissolutionThe product was dissolved in EtOAc (1 mL)
- customto evaporate
- customuntil dry
Sources & evidence
- ORD record
- ord-dbf877cf185740bc97626a5db9bbfc47
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08361998B2
Reaction notes
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