Sodium Chloride → HCID 178509115, compound
Reaction equation
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([CH:7]2[CH2:12][CH2:11][N:10](C(=O)C)[CH2:9][CH2:8]2)[C:3]=1[C:16]1[S:17][C:18]2[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=2[N:20]=1.[OH-].[Na+].[Na+].[Cl-]>Cl>[NH3:1].[S:17]1[C:18]2[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=2[N:20]=[C:16]1[C:3]1[C:4]([CH:7]2[CH2:8][CH2:9][NH:10][CH2:11][CH2:12]2)=[N:5][NH:6][C:2]=1[NH2:1]Participants
Reactant 3
Product 2
Reagents, catalysts & solvents 1
Procedure
A solution of the above prepared 1-[4-(5-amino-4-benzothiazol-2-yl-1H-pyrazol-3-yl)-piperidin-1-yl]-ethanone (54 mg, 0.158 mmol) in 6N HCl (10 mL) was refluxed for 6 hrs and was allowed to cool to room temperature overnight. The resulting mixture was poured over crushed ice (20 mL) and the solution was adjusted to neutral pH using a 10% NaOH solution. The resulting solution was saturated with NaCl and was extracted with ethyl acetate (10×50 mL). The combined extracts were washed once with brine, dried over anhydrous sodium sulfate, filtered and evaporated. The resulting crude product was purified by flash column chromatography eluting with CH2Cl2:MeOH=20:1 with 1% ammonia to yield 15 mg (32%) of the title compound. MS (m/z, ES+): 300.14 (M+1, 100%).
Workup
- temperaturewas refluxed for 6 hrs
- additionThe resulting mixture was poured
- extractionwas extracted with ethyl acetate (10×50 mL)
- washThe combined extracts were washed once with brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- customevaporated
- customThe resulting crude product was purified by flash column chromatography
- washeluting with CH2Cl2
Sources & evidence
- ORD record
- ord-92785894f6154d46b48b6de4c9b314ff
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754233B2
Reaction notes
Loading…