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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530111Generated: October 30, 2026

Triethylamine → 2-chloro-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-one

https://huagongshe.com/reaction/530111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-chloro-7-methyl-8-phenyl-7,8-dihydropteridin-6(5H)-oneHCID 89560835—
SolventDichloromethaneHCID 6344—
Product2-chloro-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-oneHCID 8957039137%

Reaction Steps

To a stirred solution of 2-chloro-7-methyl-8-phenyl-7,8-dihydropteridin-6(5H)-one (1.59 g, 5.78 mmol) in dichloromethane (75 mL) was added triethylamine (8.07 ml, 57.8 mmol), cupric acetate (2.09 g, 11.56 mmol) and phenylboronic acid (1.41 g, 11.56 mmol) followed by 4 Å molecular sieves (2 g). The resulting mixture was stirred for 48 h at rt with an air balloon on the top. The reaction mixture was then filtered over celite to give a clear solution. The solution was washed with aqueous saturated sodium bicarbonate (50 mL×2), dried over anhydrous sodium sulfate and evaporated to give a crude material, which was then purified by silica gel column chromatography (eluent: 2% methanol in dichloromethane) to give the desired product (750 mg, 37%). 1HNMR (300 MHz, CDCl3): δ 1.65 (d, J=6.9 Hz, 3H), 4.82 (q, J=6.9 Hz, 1H) and 7.36-7.65 (m, 11H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09351974B2
Source datasetuspto-grants-2016_05
ORD IDord-080b5a100755434693f4e915db85f75c
Source noteuspto-grants-2016_05