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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430511Generated: October 27, 2026

Phosphorus trichloride → 2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-one

https://huagongshe.com/reaction/430511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus trichlorideHCID 24387—
Reactant2-Chloro-3-pyridylamineHCID 80528—
Reactant3-Acetamidothiophene-2-carboxylic acidHCID 2807579—
SolventPyridineHCID 1049—
Product2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-oneHCID 1835067963%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a mixture of pyridine (4 mL), 3-amino-2-chloropyridine (0.514 g, 4 mmol), and 3-acetamidothiophene-2-carboxylic acid (0.370 g, 4 mmol) was added phosphorus trichloride (0.02 mL, 2.3 mmol). The reaction was heated to 105° C. for 3 hours, cooled to ambient temperature and partitioned between ethyl acetate and water. Phases were separated and the aqueous layer was extracted with ethyl acetate. The combined organic phase was washed with water and brine, dried over sodium sulfate and concentrated to a greenish brown oil. This residue was flash chromatographed on silica gel (20×120 mm) eluting with 20-40% ethyl acetate/hexane to afford 0.350 g (63%) of 2-methyl-3-(2-chloropyrid-3-yl)-3H-thieno[3,2-d]pyrimidin-4-one as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323208B1
Source datasetuspto-grants-2001_11
ORD IDord-2d0269e9bbed4ddebd146f92e46f6348
Source noteuspto-grants-2001_11