HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666003Generated: October 31, 2026
phenyl (3-(tert-butyl)-1-(p-tolyl)-1H-pyrazol-5-yl)carbamate → Pexmetinib
https://huagongshe.com/reaction/1666003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | phenyl (3-(tert-butyl)-1-(p-tolyl)-1H-pyrazol-5-yl)carbamate | HCID 11057211 | — |
| Reactant | 2-(5-(2-(Aminomethyl)-4-fluorophenoxy)-1H-indazol-1-yl)ethanol | HCID 44542122 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Pexmetinib | HCID 24765037 | — |
Reaction Steps
To a 4.1° C. solution of 2-(5-(2-(aminomethyl)-4-fluorophenoxy)-1H-indazol-1-yl)ethanol (71.55 g, 237 mmol) in DMA (350 mL) was added a DMA (350 mL) solution of phenyl 3-tert-butyl-1-p-tolyl-1H-pyrazol-5-ylcarbamate (80.5 g, 230 mmol). The temperature rose to 18.4° C. and stabilized. The ice bath was removed and the reaction was stirred for 2 hours. An additional portion of 2-(5-(2-(aminomethyl)-4-fluorophenoxy)-1H-indazol-1-yl)ethanol was added and the reaction was stirred for 2 hours. The reaction mixture was partitioned between isopropyl acetate (1.6 L) and water (2.4 L). The aqueous layer was removed and the organic layer was washed with 0.5 N NaOH (2×2.4 L) and then saturated brine (1×2.4 L). The organic layer was dried over Na2SO4 (300 g) and concentrated to yield 110.8 g (86.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039639B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-392efde8fe394eff838b32398456f646 |
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| Source note | uspto-grants-2011_10 |
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