(1S,3S,5S)-N-(Pyrazin-2-yl)-2-azabicyclo[3.1.0]hexane-3-carboxamide → HCID 178522396, 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.[N:18]1[CH:23]=[CH:22][N:21]=[CH:20][C:19]=1[NH:24][C:25]([C@@H:27]1[CH2:32][C@H:31]2[C@H:29]([CH2:30]2)[NH:28]1)=[O:26].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:28]2[C@H:27]([C:25]([NH:24][C:19]3[CH:20]=[N:21][CH:22]=[CH:23][N:18]=3)=[O:26])[CH2:32][C@H:31]3[C@@H:29]2[CH2:30]3)[N:7]=1Participants
4
Procedure
Compound 121D was prepared from compounds 1A and 121C using the procedure as described for 1C. LC/MS [M+H]+: 439; Ret time (Method A): 1.70 min.
Workup
- custom1.70 min.
Sources & evidence
- ORD record
- ord-ecd83d787f0b4d32bd18c650da050fe8
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415340B2
Reaction notes
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