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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853117Generated: October 26, 2026

Potassium Carbonate → 5-bromo-N-(2-(4-fluorophenyl)-2-methylpropyl)pyrimidin-2-amine

https://huagongshe.com/reaction/1853117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-fluoropyrimidineHCID 600690—
Reactant2-(4-Fluorophenyl)-2-methylpropan-1-amineHCID 21251023—
SolventIsopropanolHCID 3776—
Product5-bromo-N-(2-(4-fluorophenyl)-2-methylpropyl)pyrimidin-2-amineHCID 6745289265%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 5-bromo-2-fluoropyrimidine (1.0 g, 5.6 mmol, 1.0 equiv) and 2-(4-fluorophenyl)-2-methylpropan-1-amine (1.05 g, 6.3 mmol. 1.1 equiv) in isopropanol (12 mL) in a microwave vial equipped with a stir bar was added potassium carbonate (3.68 g, 11.2 mmol, 2.0 equiv). The vial was fitted with a microwave vial cap and heated to 120° C. for 45 min. The reaction mixture was filtered to remove the solid potassium carbonate and concentrated in vacuo. After the residue was redissolved in EtOAc and water, the organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. Purification by silica gel chromatography (3%-5% MeOH/DCM) provided the title compound as a yellow solid (1.15 g, 65%), (m/z [M+H]=324.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962632B2
Source datasetuspto-grants-2015_02
ORD IDord-9dd61d3147e04ea79f93d79345ba3dc7
Source noteuspto-grants-2015_02