Hydrochloric Acid → HCID 15484973, compound
Reaction equation
[CH2:1]([S:6]([NH2:9])(=[O:8])=[O:7])[CH2:2][CH2:3][CH2:4][CH3:5].[OH-].[Na+].[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]=[C:20]=[O:21])=[CH:15][CH:14]=1.Cl>O.CC(C)=O>[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([NH:19][C:20]([NH:9][S:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])(=[O:8])=[O:7])=[O:21])=[CH:15][CH:14]=1Participants
7
Procedure
The general method of procedure A was followed with 1-pentanesulfonamide (10 g), acetone (200 ml), 1N NaOH (66 ml) and 4-chlorophenyl isocyanate (9.6 g). 1N HCl (66 ml) was used to acidify the solution. Additional water was added and after standing overnight the solid was isolated and dried to provide 14 g of product.
Workup
- customthe solid was isolated
- customdried
Sources & evidence
- ORD record
- ord-c6a234f2f3b64409a467564d5fca5d9d
- Source dataset
- uspto-grants-2000_11
- Patent number
- US06147115
Reaction notes
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