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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421458Generated: November 1, 2026

Triethylamine → HCID 18315068, compound

https://huagongshe.com/reaction/1421458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Acetoxyisobutyroyl chlorideHCID 123496—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantHCID 18315063HCID 18315063—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
ProductHCID 18315068HCID 18315068109%

Reaction Steps

A stirred solution of 0.50 gram (0.0013 mole) of 1-methyl-6-trifluoromethyl-3-(6-amino-4-bromo-2-fluoro-5-hydroxyphenyl)-2,4(1H,3H)-pyrimidinedione, 0.21 gram (0.0013 mole) of 1-chlorocarbonyl-1-methylethyl acetate, 0.14 gram (0.0014 mole) of triethylamine, and 0.16 gram (0.0006 mole) of pyridinium p-toluenesulfonate in 50 mL of xylene was heated at 150 ° C. for about 18 hours. The reaction mixture was then cooled to ambient temperature and taken up in ethyl acetate. The solution was washed with water and an aqueous solution saturated with sodium chloride; then it was dried with magnesium sulfate. The mixture was filtered, and the filtrate was concentrated under reduced pressure to a residue. The residue was purified by column chromatography on silica gel, yielding 0.72 gram of Compound 104. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077812
Source datasetuspto-grants-2000_06
ORD IDord-c8b79b7338864d708f528a537596faff
Source noteuspto-grants-2000_06