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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272057Generated: November 3, 2026

Ethyl Acetate → HCID 58847439, compound

https://huagongshe.com/reaction/1272057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant72766-07-5HCID 12549711—
Reactant2-(Azetidin-1-ylcarbonyl)-7-chlorothieno[3,2-b]pyridineHCID 22143549—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 58847439HCID 5884743941.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of azetidin-1-yl-(7-chloro-thieno[3,2-b]pyridin-2-yl)-methanone (21a) (930 mg, 3.70 mmol), (2-chloro-4-hydroxy-phenyl)-acetic acid methyl ester (49e) (740 mg, 3.70 mmol), and Cs2CO3 (1.82 g, 7.40 mmol) in 7 mL of DMSO was heated at 100° C. for overnight and cooled to room temperature. EtOAc and water were added. The organic layer was washed three times with water, dried over Na2SO4, and concentrated in vacuo. The residue was purified by flash column chromatography eluting with EtOAc:CHCl3:MeOH (1:1:0.04) to provide 640 mg of white solid as the intermediate 49f. 1H NMR (300 MHz, CD3OD) δ 8.47 (d, 1H, J=5.46 Hz), 7.74 (s, 1H), 7.43 (d, 1H, J=8.48 Hz), 7.32 (d, 1H, J=2.45 Hz), 7.15–7.10 (m, 1H), 6.73 (d, 1H, J=5.47 Hz), 4.67–4.54 (m, 2H), 4.24–4.13 (m, 2H), 3.80 (s, 3H), 3.65 (s, 2H), 2.48–2.33 (m, 2H). LCMS (ESI+) [M+H]/z Calc'd 417, found 417.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208500B2
Source datasetuspto-grants-2007_04
ORD IDord-92bac0733db14350b6679e5c32de0bf1
Source noteuspto-grants-2007_04