Pyrrolidine → HCID 136342278, compound
Reaction equation
Cl.[C:2]1([C@@H:14]2[CH2:19][CH2:18][CH2:17][C@H:16]([NH2:20])[CH2:15]2)[N:6]2[C:7]3[CH:13]=[CH:12][NH:11][C:8]=3[N:9]=[CH:10][C:5]2=[N:4][N:3]=1.C1N=CN([C:26]([N:28]2[CH:32]=N[CH:30]=[CH:29]2)=[O:27])C=1.N1CCC[CH2:34]1>N1C=CC=CC=1>[C:2]1([C@@H:14]2[CH2:19][CH2:18][CH2:17][C@H:16]([NH:20][C:26]([N:28]3[CH2:29][CH2:30][CH2:34][CH2:32]3)=[O:27])[CH2:15]2)[N:6]2[C:7]3[CH:13]=[CH:12][NH:11][C:8]=3[N:9]=[CH:10][C:5]2=[N:4][N:3]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a flask containing cis-3-(6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyrazin-1-yl)cyclohexanamine hydrochloride (0.050 g, 0.171 mmol, Example #F.1.3) was added CDI (0.030 g, 0.188 mmol) and pyridine (2 mL). The reaction mixture was stirred at ambient temperature for about 16 h. Pyrrolidine (0.016 mL, 0.188 mmol) was added to the reaction mixture and stirred for about 16 h. The solvent was removed under reduced pressure and the crude material was purified by RP-HPLC (Table 2, Method j). The appropriate fractions were combined, the solvent was mostly removed under reduced pressure, and the solid was filtered and dried under lyophilization to give N-(cis-3-(6H-pyrrolo[2,3-e][1, 2, 4]triazolo[4,3-a]pyrazin-1-yl)cyclohexyl)pyrrolidine-1-carboxamide (0.010 g, 16%): LC/MS (Table 2, Method a) Rt=1.45 min; MS m/z 354 (M+H)+.
Workup
- stirringstirred for about 16 h
- customThe solvent was removed under reduced pressure
- customthe crude material was purified by RP-HPLC (Table 2, Method j)
- customthe solvent was mostly removed under reduced pressure
- filtrationthe solid was filtered
- customdried under lyophilization
Sources & evidence
- ORD record
- ord-e5806f4100ec4023ad9c74fd17deb85a
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08962629B2
Reaction notes
Loading…