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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426251Generated: October 31, 2026

Sodium Carbonate → 4-Chloro-5-cyclopropyl-2,6-dimethoxy-pyrimidine

https://huagongshe.com/reaction/426251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantChlorineHCID 24526—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant5-Bromo-4-chloro-2,6-dimethoxypyrimidineHCID 12226195—
CatalystPalladiumHCID 23938—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-5-cyclopropyl-2,6-dimethoxy-pyrimidineHCID 5918475765.2%

Reaction Conditions

Temperature130 °C

Reaction Steps

In a 5 mL microwave reaction tube, 5-bromo-4-chloro-2,6-dimethoxy-pyrimidine (116 mg, 0.457 mmol), cyclopropyl boronic acid (47 mg, 0.549 mmol, 1.2 eq.) and Pd(dppf(Cl2 (38 mg, 0.1 eq.) was charged with DME (2.5 mL) and 2M Na2CO3 aqueous solution (0.91 mL, 4 eq.). The reaction was heated at 130° C. in the microwave reactor for 30 minutes. Ethyl acetate was added, followed by washing with brine. The organic layer was concentrated down and purified (silica gel, 0-50% EtOAC/hexane) to give white solid (64 mg, 65%). LC-MS shows 215.1 (M+1). 1H NMR (300 MHz, CDCl3): δ 3.98 (dd, 6H), 1.62 (m, 1H), 0.99 (m, 2H), 0.78 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106064B2
Source datasetuspto-grants-2012_01
ORD IDord-c5ba8d2c36214879b6a22c42ec5498a5
Source noteuspto-grants-2012_01