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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377151Generated: October 25, 2026

Water → N-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamide

https://huagongshe.com/reaction/2377151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantN-(azetidin-3-yl)acetamideHCID 13401968—
Reactant5-[2-(3-Chloropropyloxy)ethyl]benzo[b]thiopheneHCID 21990069—
SolventDimethylformamideHCID 6228—
ProductN-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamideHCID 2354558137.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

In 8 mL of N,N-dimethylformamide was dissolved 0.80 g of 5-[2-(3-chloropropoxy)ethyl]-1-benzothiophene, and 1.20 g of N-(3-azetidinyl)acetamide was added to the solution, after which the resulting mixture was stirred at 90° C. for 12 hours. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform:methanol=7:1) to obtain 0.39 g of N-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamide as a light-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468443B2
Source datasetuspto-grants-2008_12
ORD IDord-f84111d866654a2fb57d332e3a84508c
Source noteuspto-grants-2008_12