Methanesulfonyl chloride → HCID 178484841, compound
Reaction equation
Cl.[F:2][C:3]1[CH:4]=[CH:5][C:6]([N+:18]([O-:20])=[O:19])=[C:7]([CH:17]=1)[O:8][C@H:9]1[CH2:14][CH2:13][C@H:12]([NH:15][CH3:16])[CH2:11][CH2:10]1.[CH3:21][S:22](Cl)(=[O:24])=[O:23]>>[F:2][C:3]1[CH:4]=[CH:5][C:6]([N+:18]([O-:20])=[O:19])=[C:7]([CH:17]=1)[O:8][C@H:9]1[CH2:14][CH2:13][C@H:12]([N:15]([CH3:16])[S:22]([CH3:21])(=[O:24])=[O:23])[CH2:11][CH2:10]1Participants
3
Procedure
Prepared analogously to example IV.3 from 0.305 g trans-[4-(5-fluoro-2-nitrophenoxy)-cyclohexyl]-methyl-amine hydrochloride and methanesulfonyl chloride.
Sources & evidence
- ORD record
- ord-291195f996794c2fb8c159508eefd271
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754079B2
Reaction notes
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