2-Cyclohexylethanesulfonyl chloride → Tert-butyl 3-(3-(2-cyclohexylethylsulfonamido)phenyl)propylcarbamate
Reaction equation
C1(C[NH:8][C:9]2[CH:10]=[C:11]([CH2:15][CH2:16][CH2:17][NH:18][C:19](=[O:25])[O:20][C:21]([CH3:24])([CH3:23])[CH3:22])[CH:12]=[CH:13][CH:14]=2)CCCCC1.[CH:26]1([CH2:32][CH2:33][S:34](Cl)(=[O:36])=[O:35])[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1>>[CH:26]1([CH2:32][CH2:33][S:34]([NH:8][C:9]2[CH:10]=[C:11]([CH2:15][CH2:16][CH2:17][NH:18][C:19](=[O:25])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])[CH:12]=[CH:13][CH:14]=2)(=[O:36])=[O:35])[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1Participants
3
Procedure
Sulfonation of aniline 17 by 2-cyclohexylethanesulfonyl chloride following the method used in Example 6 gives tert-butyl 3-(3-(2-cyclohexylethylsulfonamido)phenyl)propylcarbamate.
Sources & evidence
- ORD record
- ord-aa6986b81ef34093ba69290a342608a2
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09193669B2
Reaction notes
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