Methanesulfonamide → HCID 69780760, compound
Reaction equation
[C:1]1([C:7]2[CH2:8][O:9][C:10]3[C:15]([C:16]=2[C:17]2[CH:22]=[CH:21][C:20]([CH:23]=[CH:24][C:25]([OH:27])=O)=[CH:19][CH:18]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:28][S:29]([NH2:32])(=[O:31])=[O:30]>>[C:1]1([C:7]2[CH2:8][O:9][C:10]3[C:15]([C:16]=2[C:17]2[CH:22]=[CH:21][C:20]([CH:23]=[CH:24][C:25]([NH:32][S:29]([CH3:28])(=[O:31])=[O:30])=[O:27])=[CH:19][CH:18]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
Prepared by coupling 3d and methylsulfonamide in accordance with Procedure 1, Method A described hereinabove. Yield (35%); ESI m/z: 430 (M−H−, 100%).
Workup
- customPrepared
- customYield (35%)
Sources & evidence
- ORD record
- ord-5da6ab6438c2419d9092908aa53b7514
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07323587B2
Reaction notes
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