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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421922Generated: November 3, 2026

Diisopropylethylamine → HCID 67243364, compound

https://huagongshe.com/reaction/2421922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22349857HCID 22349857—
Reactant1-(4-Chlorobutyl)-3-methoxy-1H-pyridin-2-oneHCID 59234647—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventWater ethylacetateHCID 22728543—
ProductHCID 67243364HCID 6724336458.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 1-(4-chlorobutyl)-3-methoxy-1H-pyridin-2-one (0.93 mmol, 0.20 g) from Example 5.1, 2-tert-butyl-4-piperazin-1-yl-6-propylpyrimidine (0.93 mmol, 0.24 g; prepared as described in DE 19735410), sodium bromide (4.64 mmol, 0.48 g), ethyldiisopropylamine (9.09 mmol, 1.17 g) and N-methylpyrrolidinone (0.5 ml) was heated at 120° C. for 6 hours. The resulting suspension was filtered with suction and the filtrate was concentrated. The residue obtained in this way was taken up in ethyl acetate/water. The aqueous mixture was adjusted to pH 5.5 with sodium bicarbonate and the aqueous mixture was extracted several times with diethyl ether. The organic phase was then dried, the desiccant was removed by filtration, and the organic phase was concentrated under reduced pressure. Chromatography of the residue on silica gel (eluent: CH2Cl2/CH3OH (0-2%) afforded 0.24 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960386B2
Source datasetuspto-grants-2011_06
ORD IDord-52763a820e1b4e8d83697f49536ce0a7
Source noteuspto-grants-2011_06