Water → HCID 10193659, compound
Reaction equation
[C:1]([NH:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][CH:14]=1)[C:11]([S:15](Cl)(=[O:17])=[O:16])=[CH:10][CH:9]=[CH:8]2)(=[O:3])[CH3:2].[CH2:19]([NH2:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C(N(CC)CC)C.[OH2:34]>O1CCCC1>[C:25]([O:3][CH2:1][CH3:2])(=[O:34])[CH3:20].[CH:5]([O:34][CH:20]([CH3:21])[CH3:19])([CH3:6])[CH3:14].[C:1]([NH:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][CH:14]=1)[C:11]([S:15]([NH:26][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)(=[O:17])=[O:16])=[CH:10][CH:9]=[CH:8]2)(=[O:3])[CH3:2]Participants
7
Procedure
6-(Acetylamino)naphthalene-1-sulfonyl chloride (280 mg, 0.987 mmol) was added to a solution of benzylamine (127 mg, 1.19 mmol) and triethylamine (0.17 ml, 1.22 mmol) in tetrahydrofuran (3.0 ml), and the mixture was stirred at room temperature for 1 hour. Water (10 ml) was added to the reaction solution, and after the mixture was stirred for 10 minutes, the resulting solid was collected. The solid was washed with water and a mixed solvent of ethyl acetate/isopropyl ether (1/1) to give the title compound as a white solid (284 mg, 81.1%).
Workup
- stirringafter the mixture was stirred for 10 minutes
- customthe resulting solid was collected
- washThe solid was washed with water
Sources & evidence
- ORD record
- ord-1b45e07e80f24c64bd300a3ab89abd45
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07598418B2
Reaction notes
Loading…