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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860041Generated: October 30, 2026

Potassium Carbonate → HCID 58765530, compound

https://huagongshe.com/reaction/860041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Diamino-6-chloropyrimidineHCID 67432—
ReactantEthyl 4-pentenoateHCID 74786—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventDimethylformamideHCID 6228—
ProductHCID 58765530HCID 58765530—

Reaction Conditions

Temperature90 °C

Reaction Steps

Ethyl 4-pentenoate (4.93 gm, 38.4 mmol) was treated with 9-BBN (92.2 mL, 46.1 mmol; 0.5M in THF) at room temperature for 16 hours. To this solution was added Pd(OAc)2 (863 mg, 3.84 mmol), 6-chloro-2,4-diaminopyrimidine (2-1, 5.0 g, 34.6 mmol), K2CO3 (7.95 g, 57.6 mmol), 1,1′-bis(diphenylphosphino)-ferrocene (2.13 g, 3.84 mmol) and DMF (100 mL). The mixture was degassed with argon for 10 minutes then heated to 90° C. for 24 hours. The reaction mixture was cooled and stirred with ethanolamine (10 mL) for 1 hour. The volatiles were removed in vacuo and the black tarry residue was partitioned between water and EtOAc. After extraction with EtOAc (4×), the organic layers were washed with water (4×), then brine, dried (MgSO4) and concentrated. Purification by silica gel chromatography (5% MeOH in CHCl3) afforded the title compound 2-2 as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153862B2
Source datasetuspto-grants-2006_12
ORD IDord-5598bed4a6234151a378c0d39cdd8952
Source noteuspto-grants-2006_12