Acetyl chloride → HCID 68724463, compound
Reaction equation
[C:1](Cl)(=[O:3])[CH3:2].[NH2:5][CH2:6][CH:7]1[CH2:12][CH2:11][CH:10]([NH:13][S:14]([C:17]2[CH:22]=[C:21]([C:23]3[C:24]([CH3:30])=[N:25][C:26]([NH2:29])=[N:27][CH:28]=3)[CH:20]=[CH:19][C:18]=2[Cl:31])(=[O:16])=[O:15])[CH2:9][CH2:8]1>N1C=CC=CC=1>[NH2:29][C:26]1[N:25]=[C:24]([CH3:30])[C:23]([C:21]2[CH:20]=[CH:19][C:18]([Cl:31])=[C:17]([S:14]([NH:13][CH:10]3[CH2:9][CH2:8][CH:7]([CH2:6][NH:5][C:1](=[O:3])[CH3:2])[CH2:12][CH2:11]3)(=[O:16])=[O:15])[CH:22]=2)=[CH:28][N:27]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Acetyl chloride (0.045 ml, 0.066 mmol) is added to a stirred solution of N-(4-aminomethyl-cyclohexyl)-5-(2-amino-4-methyl-pyrimidin-5-yl)-2-chloro-benzenesulfonamide (Example 3-18) (0.090 g, 0.22 mmol) in dry pyridine (1 ml). After 30 min the reaction mixture is absorbed on silica and the product is purified by chromatography on silica, eluting with ethyl acetate to afford the title compound.
Workup
- customAfter 30 min the reaction mixture is absorbed on silica
- customthe product is purified by chromatography on silica
- washeluting with ethyl acetate
Sources & evidence
- ORD record
- ord-ba2870fc1d8e4c1dba6a60dd412fff1f
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263585B2
Reaction notes
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