Potassium Carbonate → HCID 86663918, compound
Reaction equation
[CH3:1][C:2]1[C:10]2[N:9]=[C:8]([C@@H:11]3[CH2:15][CH2:14][CH2:13][O:12]3)[NH:7][C:6]=2[CH:5]=[C:4]([OH:16])[CH:3]=1.[Cl:17][C:18]1[CH:23]=[C:22](Cl)[N:21]=[CH:20][N:19]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[Cl:17][C:18]1[N:19]=[CH:20][N:21]=[C:22]([O:16][C:4]2[CH:3]=[C:2]([CH3:1])[C:10]3[N:9]=[C:8]([C@@H:11]4[CH2:15][CH2:14][CH2:13][O:12]4)[NH:7][C:6]=3[CH:5]=2)[CH:23]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
135 mg (0.62 mmol) (S)-4-methyl-2-(tetrahydrofuran-2-yl)-1H-benzo[d]imidazol-6-ol and 97 mg (0.63 mmol) 4,6-dichloropyrimidine in 2.0 mL DMF were combined with 97 mg (0.70 mmol) potassium carbonate and stirred overnight at 50° C. Then ice water was added and the mixture was extracted with ethyl acetate. The organic phase was concentrated by rotary evaporation i.vac.
Workup
- extractionthe mixture was extracted with ethyl acetate
- concentrationThe organic phase was concentrated by rotary evaporation i.vac
Sources & evidence
- ORD record
- ord-d1b6d4742ccc441d87206dc3be861d8b
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08952014B2
Reaction notes
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