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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357546Generated: November 1, 2026

Water → HCID 18186469, compound

https://huagongshe.com/reaction/1357546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 18186468HCID 18186468—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 18186469HCID 1818646949.7%

Reaction Steps

Phenylboronic acid (240 mg, 2 mmol) and tetrakis(triphenylphosphine)palladium(0) (30 mg) were added to a solution of 4-anilino-2-chloro-5-iodopyrimidine (Method 59, 331 mg, 1 mmol) in toluene (10 ml) and ethanol (2.5 ml). 2M aqueous sodium carbonate solution (10 ml) was added and the mixture was stirred and heated under reflux for 3 hours. Further portions of phenylboronic acid (240 mg, 2 mmol) and tetrakis(triphenylphosphine) palladium(0) (30 mg) were added and the mixture was stirred and heated under reflux for 20 hours. The mixture was poured into water (100 ml) and extracted with ethyl acetate (2×50 ml). The combined extracts were washed with water (2×50 ml) and saturated sodium chloride (50 ml) and dried. Volatile material was removed by evaporation and the residue was purified by bond elute chromatography, eluting with 10-25% ethyl acetate in isohexane, to give the product (140 mg). NMR (CDCl3): 6.85 (s, 1H), 7.1 (t, 1H), 7.3 (t, 2H), 7.4 (m, 2H), 7.5-7.6 (m, 6H), 8.05 (s, 1H); MS (MH+): 282, 284.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593326B1
Source datasetuspto-grants-2003_07
ORD IDord-dd68c7e09a834fe596f9732c205b7d4c
Source noteuspto-grants-2003_07