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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852903Generated: October 27, 2026

Sodium Carbonate → 2-Chloro-4-(thiophen-3-yl)pyrimidine

https://huagongshe.com/reaction/852903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,4-DichloropyrimidineHCID 77531—
ReactantThiophene-3-boronic acidHCID 581760—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
Product2-Chloro-4-(thiophen-3-yl)pyrimidineHCID 1411794288.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 3-thiopheneboronic acid (500 mg, 3.91 mmol) and 2,4-dichloropyrimidine (1.16 g, 7.81 mmol) in acetonitrile (20 mL) was added a 0.4 M solution of Na2CO3 (20 mL) followed by Pd(PPh3)4 (450 mg, 0.39 mmol). The suspension was degassed and heated at 90° C. for 16 h under nitrogen, cooled down, concentrated and extracted with EtOAc. Organic layer was successively washed with saturated solution of NH4Cl, brine, dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by flash chromatography on silica gel (EtOAc/CH2Cl2: 2/98) to afford the title compound 14 (680 mg, 3.46 mmol, 88% yield). 1H NMR: (400 MHz, CDCl3) δ (ppm): 8.56 (d, J=5.2 Hz, 1H), 8.19 (dd, J=3.2, 1.2 Hz, 1H), 7.66 (dd, J=5.2, 1.2 Hz, 1H), 7.46 (d, J=5.2 Hz, 1H), 7.43 (dd, J=5.2, 2.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253204B2
Source datasetuspto-grants-2007_08
ORD IDord-b49070a6df3e441fa065774ef040255d
Source noteuspto-grants-2007_08