3,3,4,4-Tetrafluoropyrrolidine Hydrochloride → HCID 86676786, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[N:9]1[CH2:14][CH2:13][N:12]([C:15]([C:17]2[CH:22]=[CH:21][C:20]([N:23]3[C:27](=[O:28])[CH2:26][CH:25]([C:29]([OH:31])=O)[CH2:24]3)=[CH:19][CH:18]=2)=[O:16])[CH2:11][CH2:10]1.Cl.[F:33][C:34]1([F:41])[C:38]([F:40])([F:39])[CH2:37][NH:36][CH2:35]1>>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[N:9]1[CH2:10][CH2:11][N:12]([C:15]([C:17]2[CH:22]=[CH:21][C:20]([N:23]3[CH2:24][CH:25]([C:29]([N:36]4[CH2:37][C:38]([F:40])([F:39])[C:34]([F:41])([F:33])[CH2:35]4)=[O:31])[CH2:26][C:27]3=[O:28])=[CH:19][CH:18]=2)=[O:16])[CH2:13][CH2:14]1Participants
3
Procedure
Using 1-{4-[4-(2,4-dimethylphenyl)piperazine-1-carbonyl]phenyl}-5-oxopyrrolidine-3-carboxylic acid (100 mg) described in Example 333 and 3,3,4,4-tetrafluoropyrrolidine hydrochloride (43 mg) and by the reaction and treatment in the same manner as in Example 86, the title compound (40 mg) was obtained.
Sources & evidence
- ORD record
- ord-f15eef7c87d54a36af8a04999270328f
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08816079B2
Reaction notes
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