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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858539Generated: October 29, 2026

5-Bromopyrimidine → HCID 21876226, compound

https://huagongshe.com/reaction/858539

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromopyrimidineHCID 78344—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21875769HCID 21875769—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 21876226HCID 2187622650.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2-{4-[2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzimidazol-1-yl]phenyl}ethanol (step 1, 100 mg, 0.26 mmol) and 5-bromopyrimidine (45 mg, 0.28 mmol) in 1,2-dimethoxyethane (3.5 ml) was added sat. NaHCO3 aq. (1.2 ml) and Pd(PPh3)4 (60 mg, 0.05 mmol). This mixture was stirred at 70° C. for 17 h. The reaction mixture was diluted with water and extracted with CH2Cl2 (3×10 ml). The organic layer was dried (MgSO4) and concentrated to give light brown oil. This mixture was purified by SiO2 preparative TLC (CH2Cl2/methanol=10/1) to afford 45 mg (50%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148234B2
Source datasetuspto-grants-2006_12
ORD IDord-f03084a5f07e427db74a344451403dca
Source noteuspto-grants-2006_12