HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879143Generated: October 27, 2026
Ammonium Hydroxide → 5-Amino-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid
https://huagongshe.com/reaction/879143
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 5-Bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid | HCID 66652334 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Carbon Dioxide | HCID 280 | — |
| Product | 5-Amino-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid | HCID 66652343 | — |
Reaction Steps
CuSO4 (0.1 eq) was added to a mixture of 5-bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid (1 eq) and 28% aqueous ammonium hydroxide solution in a microwave reaction vessel. The reaction mixture was heated in a microwave reactor at 110° C. for 25 min. The reaction vessel was cooled in dry ice for 30 min then unsealed and concentrated in vacuo. To the resulting solids was added 1.0 N HCl and the mixture was extracted with EtOAc. Combined organic extracts were washed once with brine, then dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give 5-amino-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid. The crude product was used for the next step without further purification. LCMS (m/z): 252.0 (MH+), Rt=2.0 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987457B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-9b6b3b128dd24588b93ce8280444ff20 |
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| Source note | uspto-grants-2015_03 |
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