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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030061Generated: November 4, 2026

Ethyl 4-chloro-2-methylpyrimidine-5-carboxylate → Ethyl 2-methyl-4-{N-butyl-N-[{2'-(N-triphenylmethyltetrazol-5-yl)biphenyl-4-yl}methyl]amino}pyrimidine-5-carboxylate

https://huagongshe.com/reaction/1030061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloro-2-methylpyrimidine-5-carboxylateHCID 12677176—
ReactantN-Triphenylmethyl-5-(4'-butylaminomethylbiphenyl-2-yl)tetrazoleHCID 19821739—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductEthyl 2-methyl-4-{N-butyl-N-[{2'-(N-triphenylmethyltetrazol-5-yl)biphenyl-4-yl}methyl]amino}pyrimidine-5-carboxylateHCID 19791910—

Reaction Steps

The product of Example 1A was dissolved in 15 ml of THF containing 4.6 ml of triethylamine. A solution of 1.94 g (9.7 mmoles) of ethyl-2-methyl-4-chloropyrimidine-5-carboxylate (E. Peters, et al., J. Org. Chem. 25 2137 (1960)) in 2 ml of THF was added and the resulting solution was stirred at room temperature for 2 hours. The solution was then concentrated and the resulting residue was dissolved in toluene. The toluene solution was extracted with potassium bicarbonate, dried over sodium sulfate and concentrated. The crude product was chromatographed on silica gel eluting with 12% ethyl acetate/88%toluene to provide 4.97 g of the desired product, which was crystallized from ether/hexane (1:1). M.p. 130°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104877
Source datasetuspto-grants-1992_04
ORD IDord-5498374cdf08456bb3e5493066efbb95
Source noteuspto-grants-1992_04