Hydrochloric Acid → 2-(4-chloro-3-(4-fluorophenyl)-5-phenyl-1H-pyrazolo[3,4-c]pyridazin-1-yl)acetic acid
Reaction equation
[N:1]([O-])=O.[Na+].[NH2:5][C:6]1[N:10]([CH2:11][C:12]([OH:14])=[O:13])[N:9]=[C:8]([C:15]2[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=2)[C:7]=1[C:22]#[C:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.[ClH:30]>>[Cl:30][C:22]1[C:23]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[N:1][N:5]=[C:6]2[N:10]([CH2:11][C:12]([OH:14])=[O:13])[N:9]=[C:8]([C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)[C:7]=12Participants
4
Conditions
- Temperature
- -5 °C
Procedure
To a cooled (cooling bath −5° C.) stirred suspension of sodium nitrite (320 mg, 4.65 mmol) in conc. HCl (5 mL) was added 2-(5-amino-3-(4-fluorophenyl)-4-(phenylethynyl)-1H-pyrazol-1-yl)acetic acid (521 mg, 1.55 mmol). A further 5 ml of conc. HCl was added and the cooling bath was removed and the reaction mixture was stirred at room temperature for 3.5 h. Water and CH2Cl2 were added to the reaction mixture. The aqueous phase was extracted with CH2Cl2 and the organic phases combined, dried over MgSO4, filtered and evaporated to give 2-(4-chloro-3-(4-fluorophenyl)-5-phenyl-1H-pyrazolo[3,4-c]pyridazin-1-yl)acetic acid as a solid (419 mg), which was used as such in the subsequent step.
Workup
- temperatureTo a cooled
- customthe cooling bath was removed
- stirringthe reaction mixture was stirred at room temperature for 3.5 h
- additionWater and CH2Cl2 were added to the reaction mixture
- extractionThe aqueous phase was extracted with CH2Cl2
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated
Sources & evidence
- ORD record
- ord-a68c259d6827475d9db174fc464967a2
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09260381B2
Reaction notes
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