Hydrochloric Acid → HCID 178522519, compound
Reaction equation
[C:1]1([C:7]2[C:14]3[S:13][C:12]([NH2:15])=[N:11][C:10]=3[NH:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N1C=CC=CC=1.Cl.[C:23](Cl)(=[O:30])[C:24]1[CH:29]=[CH:28][N:27]=[CH:26][CH:25]=1.[OH-].[Na+].Cl>C1COCC1.CO>[C:1]1([C:7]2[C:14]3[S:13][C:12]([NH:15][C:23](=[O:30])[C:24]4[CH:29]=[CH:28][N:27]=[CH:26][CH:25]=4)=[N:11][C:10]=3[NH:9][N:8]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 70 °C
Procedure
To a stirring solution of 3-phenyl-1H-pyrazolo[3,4-d]thiazol-5-ylamine (20 mg, 0.092 mmol) and pyridine (52 μL, 0.65 mmol) in THF (0.5 mL) was added isonicotinoyl chloride hydrochloride (82 mg, 0.46 mmol). The reaction mixture was stirred at 70° C. for 22 h, then cooled to room temperature and treated with MeOH (1 mL) and a 4N aqueous solution of NaOH (0.25 mL). The reaction mixture was further stirred at room temperature for 4 h, then a 1N aqueous solution of HCl was added to adjust the pH to 7, and the mixture was extracted with 10% MeOH in CH2Cl2 (3×). Purification on silica gel with 0-10% MeOH in CH2Cl2 as eluent provided 12.5 mg (42%) of N-(3-phenyl-1H-pyrazolo[3,4-d]thiazol-5-yl)-isonicotinamide as a beige solid. 1H-NMR (d6-DMSO) δ: 13.5 and 13.7 (2 broad s, 1H, NH+tautomer), 13.2 (broad s, 1H, NH), 8.83 (d, 2H), 7.99 (d, 2H), 7.80 (m, 2H, tautomers), 7.55 (m, 2H, tautomers), 7.40 (m, 1H, tautomers; HPLC/MS m/z: 322 [MH]+.
Workup
- temperaturecooled to room temperature
- stirringThe reaction mixture was further stirred at room temperature for 4 h
- extractionthe mixture was extracted with 10% MeOH in CH2Cl2 (3×)
- customPurification on silica gel with 0-10% MeOH in CH2Cl2 as eluent
Sources & evidence
- ORD record
- ord-5c14d7f584054668afc487683f8026ad
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07473783B2
Reaction notes
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