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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733200Generated: October 30, 2026

4-Propyl-6-trimethylstannanyl-pyrimidine-2-carbonitrile → 4-(3-Cyclopentylphenyl)-6-propylpyrimidine-2-carbonitrile

https://huagongshe.com/reaction/733200

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Propyl-6-trimethylstannanyl-pyrimidine-2-carbonitrileHCID 69049300—
Reactant1-Cyclopentyl-3-iodobenzeneHCID 69050595—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product4-(3-Cyclopentylphenyl)-6-propylpyrimidine-2-carbonitrileHCID 4688144936%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-cyclopentyl-3-iodo-benzene (158 mg, 0.58 mmol), 4-propyl-6-trimethylstannanyl-pyrimidine-2-carbonitrile (150 mg, 0.48 mmol) and PdCl2(PPh3)2 (34 mg, 0.05 mmol) in dry DMF (3 ml) was heated to 80° C. for 6 h under a nitrogen atmosphere. More catalyst (40 mg, 0.06 mmol) was added and the mixture was heated for 12 h at 80° C. The solvent was removed under reduced pressure and the residue was partitioned between water (5 ml) and AcOEt (5 ml). The aqueous layer was extracted twice with AcOEt (2×5 ml). The combined organic layers were washed with brine, dried over MgSO4 and concentrated under reduced pressure to give 272 mg of crude product which was purified by silica gel chromatography (eluent:cyclohexane/AcOEt 95/5) to give the above titled compound: 51 mg, yield: 36%, HPLC: 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589095B2
Source datasetuspto-grants-2009_09
ORD IDord-0090e022bdd741e3bf693d0ec3078038
Source noteuspto-grants-2009_09