Pyrrolidine → HCID 136342278, compound

HRID 1854358Notes

Reaction equation

HRID 1854358 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]=1

Participants

5

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

  1. stirringstirred for about 16 h
  2. customThe solvent was removed under reduced pressure
  3. customthe crude material was purified by RP-HPLC (Table 2, Method j)
  4. customthe solvent was mostly removed under reduced pressure
  5. filtrationthe solid was filtered
  6. customdried under lyophilization

Sources & evidence

ORD record
ord-e5806f4100ec4023ad9c74fd17deb85a
Source dataset
uspto-grants-2015_02
Patent number
US08962629B2

Reaction notes

Loading…