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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982213Generated: October 30, 2026

Methane → 6-methyl-5-(2-methyl-4-thiazolyl)-2-(1H)-pyridinone

https://huagongshe.com/reaction/1982213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantDiethyl PhthalateHCID 6781—
Reactant1,2-Dihydro-6-methyl-5-(2-methyl-4-thiazolyl)-2-oxo-3-pyridinecarboxylic acidHCID 15592168—
Product6-methyl-5-(2-methyl-4-thiazolyl)-2-(1H)-pyridinoneHCID 1559216941.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a 100 ml portion of boiling diethyl phthalate was added 20 g of 1,2-dihydro-6-methyl-5-(2-methyl-4-thiazolyl)-2-oxo-3-pyridinecarboxylic acid and the resulting dark solution was heated for about 15 minutes and then cooled to about 150° C., treated with decolorizing charcoal and filtered. The filtrate was diluted with 350 ml of n-hexane (no solid precipitated) and then extracted with 300 ml of 3% aqueous sodium hydroxide solution. The aqueous phase was separated and acidified with acetic acid, yielding no precipitate. The acidic solution was concentrated on a rotary evaporator to a volume of about 100 ml and allowed to stand at room temperature overnight. The resulting crystalline yellow solid that had separated was collected, washed with water, dried and then recrystallized from isopropyl alcohol-ether to produce 6.8 g of 6-methyl-5-(2-methyl-4-thiazolyl)-2-(1H)-pyridinone, m.p. 188°-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04595762
Source datasetuspto-grants-1986_06
ORD IDord-4293bbc974dc403a9ff3e9ead491212f
Source noteuspto-grants-1986_06