HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986107Generated: October 31, 2026
Potassium Cyanide → 4-(4-(2-Carbamoylpyridin-4-yloxy)-3-fluorophenylamino)-2-cyano-N-(2,4-difluorophenyl)pyrimidine-5-carboxamide
https://huagongshe.com/reaction/1986107
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-(4-(2-carbamoylpyridin-4-yloxy)-3-fluorophenylamino)-N-(2,4-difluorophenyl)-2-(methylsulfonyl)pyrimidine-5-carboxamide | HCID 57721359 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-(2-Carbamoylpyridin-4-yloxy)-3-fluorophenylamino)-2-cyano-N-(2,4-difluorophenyl)pyrimidine-5-carboxamide | HCID 57721323 | 94% |
Reaction Steps
To a solution of 4-(4-(2-carbamoylpyridin-4-yloxy)-3-fluorophenylamino)-N-(2,4-difluorophenyl)-2-(methylsulfonyl)pyrimidine-5-carboxamide (200 mg, 0.36 mmol) in DMF (4 mL) was added potassium cyanide (94 mg, 1.44 mmol) and the mixture was heated to 80° C. After 5 h. The mixture was cooled to rt and the solvent was removed in vacuo. The residue was diluted with brine and extracted with EtOAc. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo to give the nitrile (171 mg, 94%) as a solid. MS(ESI+) m/z 506 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07547782B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-6d4bce38c9a24ca5a0f167b0420d5404 |
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| Source note | uspto-grants-2009_06 |
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