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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719961Generated: October 25, 2026

Pyridine → 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylic acid

https://huagongshe.com/reaction/1719961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantLithium iodideHCID 66321—
Reactantmethyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylateHCID 13060555—
SolventWaterHCID 962—
Product4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylic acidHCID 1306055922.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of methyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrmido[1,2-C]quinazoline-3-carboxylate (3.2 g), anhydrous lithium iodide (8.0 g) and dry pyridine (32 ml) was stirred at 120° C. for 1.5 hours. The reaction mixture was concentrated under reduced pressure to give a residue, which was dissolved in water. Insoluble materials were removed by filtration. The aqueous layer was adjusted to pH 1-2 with conc. hydrochloric acid to give crystals, which were separated by filtration and dried. The crude crystals were washed with methanol three times and recrystallized from acetonitrile to give 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylic acid (0.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04543356
Source datasetuspto-grants-1985_09
ORD IDord-ec6bc8db607644849617683f7e835ccc
Source noteuspto-grants-1985_09