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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333702Generated: October 29, 2026

N,N-Dimethylaniline → 4-Chloro-2-(2-methoxyphenyl)thieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/333702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(2-methoxyphenyl)thieno[3,2-d]pyrimidin-4(3H)-oneHCID 135991504—
SolventBenzeneHCID 241—
Product4-Chloro-2-(2-methoxyphenyl)thieno[3,2-d]pyrimidineHCID 5902663371.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2-(2-methoxyphenyl)thieno[3,2-d]pyrimidin-4(3H)-one (0.80 g, 3.1 mmol), POCl3 (0.28 mL, 3.1 mmol), and N,N-dimethylaniline (1.6 mL, 4.7 mmol) in benzene (3.5 mL) was heated at 80° C. for 2 h. An additional portion of POCl3 (0.28 mL, 3.1 mmol) was added, and the reaction was heated at 80° C. for 16 h. The reaction was cooled, and saturated aqueous NaHCO3 was slowly added. The organic layer was separated, washed with water, dried over Na2SO4, and concentrated under vacuum to give 4-chloro-2-(2-methoxyphenyl)thieno[3,2-d]pyrimidine (0.61 g, 71% yield). LC/MS: m/z 277.1 (M+H)+ at 2.98 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883781B2
Source datasetuspto-grants-2014_11
ORD IDord-37fd4a7dec204db6a8e96c41ff8176e4
Source noteuspto-grants-2014_11