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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Propyl-6-trimethylstannanyl-pyrimidine-2-carbonitrile | HCID 69049300 | — |
| Reactant | 1-Cyclopentyl-3-iodobenzene | HCID 69050595 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Cyclopentylphenyl)-6-propylpyrimidine-2-carbonitrile | HCID 46881449 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589095B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-0090e022bdd741e3bf693d0ec3078038 |
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| Source note | uspto-grants-2009_09 |
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