cis-2-Pyrrolidin-1-yl-cyclopentylamine → HCID 51001235, compound
Reaction equation
[N:1]1([C@H:6]2[CH2:10][CH2:9][CH2:8][C@H:7]2[NH2:11])[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:12][C:13]1[CH:21]=[C:20]([C:22]([F:25])([F:24])[F:23])[CH:19]=[C:18]([CH3:26])[C:14]=1[C:15](O)=[O:16]>>[CH3:26][C:18]1[CH:19]=[C:20]([C:22]([F:23])([F:24])[F:25])[CH:21]=[C:13]([CH3:12])[C:14]=1[C:15]([NH:11][C@@H:7]1[CH2:8][CH2:9][CH2:10][C@@H:6]1[N:1]1[CH2:2][CH2:3][CH2:4][CH2:5]1)=[O:16]Participants
3
Procedure
The title compound, light yellow oil, MS: m/e=355.3 [(M+H)+], was prepared in accordance with the general method of example 5 from cis-2-pyrrolidin-1-yl-cyclopentylamine (intermediate Q) and 2,6-dimethyl-4-trifluoromethyl-benzoic acid (intermediate AQ).
Sources & evidence
- ORD record
- ord-9a202839734444ddbebacdb920e3693e
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08080541B2
Reaction notes
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