(S)-(+)-1-(2-Pyrrolidinylmethyl)pyrrolidine → HCID 58327870, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:28]([F:31])([F:30])[F:29])=[C:6]([CH:27]=1)[CH2:7][N:8]1[CH2:13][CH2:12][NH:11][C:10]2[N:14]=[CH:15][C:16]([C:18]3[CH:19]=[C:20]([CH:24]=[CH:25][CH:26]=3)[C:21](O)=[O:22])=[CH:17][C:9]1=2.[N:32]1([CH2:37][C@@H:38]2[CH2:42][CH2:41][CH2:40][NH:39]2)[CH2:36][CH2:35][CH2:34][CH2:33]1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:28]([F:29])([F:30])[F:31])=[C:6]([CH:27]=1)[CH2:7][N:8]1[CH2:13][CH2:12][NH:11][C:10]2[N:14]=[CH:15][C:16]([C:18]3[CH:19]=[C:20]([C:21]([N:39]4[CH2:40][CH2:41][CH2:42][C@H:38]4[CH2:37][N:32]4[CH2:36][CH2:35][CH2:34][CH2:33]4)=[O:22])[CH:24]=[CH:25][CH:26]=3)=[CH:17][C:9]1=2Participants
3
Procedure
3-{1-[5-chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}benzoic acid was reacted with (S)-2-(1-pyrrolidinylmethyl)pyrrolidine as in General Procedure 10 to give the title compound. LCMS: m/z=583.96 (M+H+); retention time=0.58 minutes.
Sources & evidence
- ORD record
- ord-b035496d49594b3ebc83fe731811bfd9
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08080561B2
Reaction notes
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