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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300082Generated: November 1, 2026

N,N-dimethyl-p-phenylenediamine → C2 Pyrido[2,3-d]pyrimidin-7-one deriv. 31

https://huagongshe.com/reaction/2300082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-dimethyl-p-phenylenediamineHCID 7472—
ReactantPyrido[2,3-d]pyrimidin-7(8H)-one, 8-ethyl-2-(methylsulfinyl)-HCID 10752351—
ProductC2 Pyrido[2,3-d]pyrimidin-7-one deriv. 31HCID 533021750%

Reaction Conditions

Temperature175 °C

Reaction Steps

A mixture of 8-ethyl-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-one (155 mg, 0.65 mmol) and 500 μL of 4-dimethylaminoaniline was heated at 175° C. for 10 minutes, then cooled to room temperature and partitioned between saturated sodium bicarbonate and ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The resultant solid was washed with hexane and ethyl acetate then purified by flash chromatography eluting with ethyl acetate. The fractions containing product were concentrated and a 2:1 mixture of hexane and ethyl acetate was added to the residue. The resultant precipitate was collected by filtration to give 110 mg (50%) of 2-(4-dimethylamino-phenylamino)-8-ethyl-8H-pyrido[2,3-d]pyrimidin-7-one, mp 189-191° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498163B1
Source datasetuspto-grants-2002_12
ORD IDord-c258c07fe8264c3683bd7a261c76449c
Source noteuspto-grants-2002_12