Pyrrolidine → HCID 44196882, compound
Reaction equation
N1CCCC1.[F:6][C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[N:12]([CH2:16][C:17]([OH:19])=[O:18])[C:11]([CH3:20])=[C:10]2[CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([S:28]([N:31]2[CH2:36][CH2:35][CH2:34]C[CH2:32]2)(=[O:30])=[O:29])[CH:23]=1>>[F:6][C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[N:12]([CH2:16][C:17]([OH:19])=[O:18])[C:11]([CH3:20])=[C:10]2[CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([S:28]([N:31]2[CH2:32][CH2:34][CH2:35][CH2:36]2)(=[O:30])=[O:29])[CH:23]=1Participants
3
Procedure
Pyrrolidine was used a starting material in Procedure H, otherwise this compound was prepared in a similar manner to Compound 4, using Procedures H, I, J, K & L.
Sources & evidence
- ORD record
- ord-1f87659eeef54a2b9e4e9af120ff5a2a
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08168673B2
Reaction notes
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