Dimethylformamide → HCID 86605410, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:13]=[C:12]([C:14]2[CH:23]=[CH:22][C:17]3[O:18][CH2:19][CH2:20][O:21][C:16]=3[CH:15]=2)[N:11]([CH:24]([CH3:26])[CH3:25])[N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.P(Cl)(Cl)(Cl)=O.[OH-].[Na+].CN(C)[CH:36]=[O:37]>>[CH2:1]([O:8][C:9]1[NH:10][N:11]([CH:24]([CH3:26])[CH3:25])[C:12]([C:14]2[CH:23]=[CH:22][C:17]3[O:18][CH2:19][CH2:20][O:21][C:16]=3[CH:15]=2)([CH:36]=[O:37])[CH:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
5
Conditions
- Temperature
- 80 °C
Procedure
To a solution of 3-benzyloxy-5-(2,3-dihydrobenzo-[1,4]dioxin-6-yl)-1-isopropyl-1H-pyrazole (1.8 g) in N,N-dimethylformamide (3 mL) was added phosphorus oxychloride (0.97 g) at 80° C., and the mixture was stirred at 80° C. for 2 hours. After the reaction mixture was cooled to room temperature, a sodium hydroxide aqueous solution (2 mol/L, 10 mL) was added to the reaction mixture. The mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: hexane/dichloromethane=1/4-dichloromethane) to give the title compound (0.86 g).
Workup
- temperatureAfter the reaction mixture was cooled to room temperature
- extractionThe mixture was extracted with diethyl ether
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- customthe solvent was removed under reduced pressure
- customThe residue was purified by column chromatography on silica gel (eluent: hexane/dichloromethane=1/4-dichloromethane)
Sources & evidence
- ORD record
- ord-86d9c60b5ef14b9b81775cf5c06950d6
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07888487B2
Reaction notes
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