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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094720Generated: November 2, 2026

Thionyl Chloride → 5-methyl-6-(pyrrolidine-1-carbonyl)thieno[2,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/1094720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantPyrrolidineHCID 31268—
Reactant5-methyl-4-oxo-3H,4H-thieno[2,3-d]pyrimidine-6-carboxylic acidHCID 405802—
SolventDimethylformamideHCID 6228—
Product5-methyl-6-(pyrrolidine-1-carbonyl)thieno[2,3-d]pyrimidin-4(3H)-oneHCID 5984283165%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of pure 5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylic acid, (0.1 g, 0.47 mmol) in DMF (5 mL) was added dropwise thionyl chloride (0.034 mL, 0.47 mmol). The reaction mixture was stirred at 0° C. for 15 min. Pyrrolidine (0.12 mL, 1.4 mmol) was then added and the reaction was allowed to warm to RT over 1 h. The reaction mixture was quenched with saturated NaHCO3 (25 mL) and extracted with EtOAc (25 mL). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated to give 0.080 g of pure 5-methyl-6-(pyrrolidine-1-carbonyl)thieno[2,3-d]pyrimidin-4(3H)-one, (yield: 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133998B2
Source datasetuspto-grants-2012_03
ORD IDord-90e2ca160ddf45cfbf02abb433fa6603
Source noteuspto-grants-2012_03