Hydrogen chloride-ethyl acetate → 1-(2,6-difluorophenyl)-3-(4-(morpholin-4-yl)phenyl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one hydrochloride

HRID 2206187Notes

Reaction equation

HRID 2206187 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[N:9]1[C:17]2[CH:16]=[CH:15][NH:14][C:13](=[O:18])[C:12]=2[C:11]([C:19]2[CH:24]=[CH:23][C:22]([N:25]3[CH2:30][CH2:29][O:28][CH2:27][CH2:26]3)=[CH:21][CH:20]=2)=[N:10]1.C(OC(=O)C)C.[ClH:37]>C(O)C>[ClH:37].[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[N:9]1[C:17]2[CH:16]=[CH:15][NH:14][C:13](=[O:18])[C:12]=2[C:11]([C:19]2[CH:20]=[CH:21][C:22]([N:25]3[CH2:26][CH2:27][O:28][CH2:29][CH2:30]3)=[CH:23][CH:24]=2)=[N:10]1

Participants

4

Procedure

To a solution of 1-(2,6-difluorophenyl)-3-(4-(morpholin-4-yl)phenyl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one (500 mg) obtained in Example 179 in ethanol (4 mL) was added 4M hydrogen chloride ethyl acetate (0.612 mL), and the mixture was stirred at room temperature for 30 min. The reaction mixture was concentrated, and the residue was crystallized from DMSO and ethyl acetate to give the title compound (433 mg).

Workup

  1. concentrationThe reaction mixture was concentrated
  2. customthe residue was crystallized from DMSO and ethyl acetate

Sources & evidence

ORD record
ord-5100fb0c44e34b61a74b05c224b5805c
Source dataset
uspto-grants-2016_06
Patent number
US09371320B2

Reaction notes

Loading…