Hydrochloric Acid → HCID 21388870, compound
Reaction equation
[C:1]([NH2:9])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:10]>>[ClH:10].[CH2:4]([C:5]1[CH:6]=[CH:7][C:2]([C:1]([NH2:9])=[O:8])=[CH:3][CH:4]=1)[CH2:3][CH2:2][CH2:7][CH3:6]Participants
3
Procedure
A solution of the benzamide of part E (2.09 g, 3.4 mmol) in 4N HCl (20 mL) was stirred for 72 hours. The solution was concentrated in vacuo and the residue was dissolved into ethyl acetate (5 mL) and dropped into ethyl ether. The resulting precipitate was collected by vacuum filtration to provide R-N-[4-[[[1-carboxyl]-2-methylpropyl][2-(4-orpholinyl)ethyl]amino]-sulfonyl]phenyl]-4-pentylbenzamide monohydrochloride as white solid (1.9 g, 94%).
Workup
- concentrationThe solution was concentrated in vacuo
- dissolutionthe residue was dissolved into ethyl acetate (5 mL)
- additiondropped into ethyl ether
- filtrationThe resulting precipitate was collected by vacuum filtration
Sources & evidence
- ORD record
- ord-fb4fe40546b0470dbc1aea8b410586c8
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06869951B1
Reaction notes
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