(2S,4S)-4-Hydroxy-N-(pyrazin-2-yl)pyrrolidine-2-carboxamide → HCID 178522398, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([Cl:8])[N:5]=[C:4]([NH:9][C:10]2[NH:14][N:13]=[C:12]([CH:15]3[CH2:17][CH2:16]3)[CH:11]=2)[N:3]=1.[OH:18][C@@H:19]1[CH2:23][NH:22][C@H:21]([C:24]([NH:26][C:27]2[CH:32]=[N:31][CH:30]=[CH:29][N:28]=2)=[O:25])[CH2:20]1.ClC1N=C(NC2NN=C(C3CC3)C=2)N=C(N2CCC[C@@]2(C)C(NC2C=NC(F)=CC=2)=O)N=1>>[Cl:8][C:6]1[N:5]=[C:4]([NH:9][C:10]2[NH:14][N:13]=[C:12]([CH:15]3[CH2:17][CH2:16]3)[CH:11]=2)[N:3]=[C:2]([N:22]2[CH2:23][C@@H:19]([OH:18])[CH2:20][C@H:21]2[C:24]([NH:26][C:27]2[CH:32]=[N:31][CH:30]=[CH:29][N:28]=2)=[O:25])[N:7]=1Participants
4
Procedure
Compound 85B was prepared from 1A and 85A as described for 1C. LC/MS [M+H]+: 443/445; Ret time (Method F): 2.18 min.
Workup
- custom2.18 min.
Sources & evidence
- ORD record
- ord-c6e1fad929db4109a77e8c8117656ef9
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415340B2
Reaction notes
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