HCID 14115006, compound → HCID 69275466, compound
Reaction equation
CC1C=CC(S(N[C@H](C[C:15]#[C:16][Si:17]([CH3:20])([CH3:19])[CH3:18])C)(=O)=O)=CC=1.[F:21][C:22]1[CH:27]=[CH:26][C:25]([CH:28]2[CH2:30][N@@:29]2[S:31]([C:34]2[CH:39]=[CH:38][CH:37]=[C:36]([C:40]([F:43])([F:42])[F:41])[CH:35]=2)(=[O:33])=[O:32])=[CH:24][CH:23]=1>>[F:21][C:22]1[CH:27]=[CH:26][C:25]([C@H:28]([NH:29][S:31]([C:34]2[CH:39]=[CH:38][CH:37]=[C:36]([C:40]([F:43])([F:42])[F:41])[CH:35]=2)(=[O:33])=[O:32])[CH2:30][C:15]#[C:16][Si:17]([CH3:20])([CH3:19])[CH3:18])=[CH:24][CH:23]=1Participants
3
Procedure
Proceeding as described for (51), but using (S)-2-(4-fluorophenyl)-1-(3-(trifluoro-methyl)benzenesulfonyl)aziridine afforded (R)—N-(1-(4-fluorophenyl)-4-(trimethylsilyl)but-3-ynyl)-3-(trifluoromethyl)benzenesulfonamide (53). MS (m/z): 444.3 (M+H) (Calc'd for C20H21F4NO2SSi: 443.54).
Sources & evidence
- ORD record
- ord-2e9acca5828447389e3c2e4690cffa0a
- Source dataset
- uspto-grants-2008_08
- Patent number
- US07414134B2
Reaction notes
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