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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705231Generated: October 27, 2026

Ammonium Hydroxide → 5-Amino-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid

https://huagongshe.com/reaction/705231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant5-Bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acidHCID 66652334—
CatalystCopper SulfateHCID 24462—
SolventCarbon DioxideHCID 280—
Product5-Amino-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acidHCID 66652343—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173883B2
Source datasetuspto-grants-2015_11
ORD IDord-2cfde0008207448a9db7110ea9667be3
Source noteuspto-grants-2015_11