HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946352Generated: October 25, 2026
Potassium Hydroxide → [[(2,6-Difluorophenyl)carbonyl](1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)amino]methyl bis(1,1-dimethylethyl) phosphate
https://huagongshe.com/reaction/1946352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Di-tert-butyl (chloromethyl) phosphate | HCID 11701630 | — |
| Reactant | Gsk-5498A | HCID 46945384 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [[(2,6-Difluorophenyl)carbonyl](1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)amino]methyl bis(1,1-dimethylethyl) phosphate | HCID 59547970 | — |
Reaction Steps
A solution of 2,6-difluoro-N-(1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)benzamide (for a preparation see Example 29)(61.25 g, 153 mmol), chloromethyl bis(1,1-dimethylethyl) phosphate (for a preparation see Intermediate 60)(47.6 g, 184 mmol) and potassium hydroxide (14.18 g, 215 mmol) in N,N-dimethylformamide (500 ml) was stirred at ambient temperature for 7 days. The reaction mixture was partitioned between ethyl acetate (350 ml) and water/brine (250 ml, 1:1 volume/volume). The organic phase was washed with brine (250 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The sample was loaded in dichloromethane and purified on a silica Redisep cartridge 1500 g using a gradient of 0-75% ethyl acetate-cyclohexane over 8 column volumes. The appropriate fractions were combined and evaporated in vacuo to give the title compound as a colourless gum (which started to crystallise to a white solid (72.44 g); LCMS: (System 8) MH+=622, tRET=3.40 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08399436B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-40daeab8295542e8b7ad97be4a230473 |
|---|
| Source note | uspto-grants-2013_03 |
|---|