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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354870Generated: October 30, 2026

Pyridine → Diethyl [(6-isobutyramido-4-quinazolinylamino)methylene]propanedioate

https://huagongshe.com/reaction/354870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantIsobutyryl chlorideHCID 62325—
ReactantDiethyl[(6-amino-4-quinazolinylamino)methylene]propanedioateHCID 20266113—
SolventDichloromethaneHCID 6344—
ProductDiethyl [(6-isobutyramido-4-quinazolinylamino)methylene]propanedioateHCID 1306048742.2%

Reaction Steps

A mixture of diethyl [(6-amino-4-quinazolinylamino)methylene]propanedioate (2.5 g), pyridine (1.2 g) and dichloromethane (55 ml) was stirred under ice-cooling. To the reaction mixture was added dropwise isobutyryl chloride (1.06 g). The reaction mixture was stirred under ice-cooling for 30 minutes and at ambient temperature for 20 minutes. After ice-water was added to the reaction mixture, the resultant mixture was stirred and extracted with chloroform. Insoluble materials were removed by filtration from the extracts. The extracts were washed three times with water and with aqueous solution saturated with sodium chloride, dried over magnesium sulfate and concentrated under reduced pressure. The resultant residue was purified by a column chromatography using silica gel (developing solvent: chloroform) and crystallized from a mixture of chloroform and hexane to give crystalline diethyl [(6-isobutyramido-4-quinazolinylamino)methylene]propanedioate (1.28 g). Crystals (0.67 g) of the same compound were recovered from the mother liquor by substantially the same crystallization as mentioned above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377580
Source datasetuspto-grants-1983_03
ORD IDord-e889895ee17943ba91cb4d55a10d8c00
Source noteuspto-grants-1983_03