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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354881Generated: October 30, 2026

Diphenyl Ether → HCID 13060552, compound

https://huagongshe.com/reaction/354881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl EtherHCID 7583—
ReactantHCID 13060511HCID 13060511—
SolventHexaneHCID 8058—
ProductHCID 13060552HCID 1306055281.4%

Reaction Conditions

Temperature260 °C

Reaction Steps

A mixture of dimethyl [{6-pivalamido--4-quinazolinylamino}methylene]propanedioate (24.5 g) and diphenyl ether (150 ml) was heated at 260° C. for 20 minutes and cooled to ambient temperature. To the reaction mixture was added hexane to give crystals, which were filtered off, washed with hexane and dissolved in chloroform (400 ml) under heating. Insoluble materials were removed by filtration. The filtrate was concentrated under reduced pressure to 200 ml and allowed to stand under cooling. The precipitated crystals were filtered off and washed with chloroform to give crystalline methyl 4-oxo-10-pivalamido--4H-pyrimido[1,2-c]quinazoline-3-carboxylate (18.29 g). The mother liqour was concentrated under reduced pressure to give crystals, which were purified by a column chromatography on silica gel (50 g) (Developing solvent: 5% methanol-chloroform solution) and recrystallized from chloroform to give the same object compound (3.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377580
Source datasetuspto-grants-1983_03
ORD IDord-ff88f035607e46ac9c0c87e42b92c415
Source noteuspto-grants-1983_03