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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602328Generated: October 26, 2026

Sodium Bicarbonate → N-[4-(3-oxomorpholin-4-yl)phenyl]-3-(5-chlorothiophene-2-carbonyl)oxazolidine-5-carboxamide

https://huagongshe.com/reaction/602328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(4-Aminophenyl)morpholin-3-oneHCID 11194854—
Reactant3-(5-Chlorothiophene-2-carbonyl)oxazolidine-5-carboxylic acidHCID 58691249—
SolventDimethylformamideHCID 6228—
ProductN-[4-(3-oxomorpholin-4-yl)phenyl]-3-(5-chlorothiophene-2-carbonyl)oxazolidine-5-carboxamideHCID 11604507—

Reaction Steps

4.2 479 mg (2.50 mmol) of N-(3-dimethylaminopropyl)-N′-ethyl-carbodiimide hydrochloride (DAPECI) are added to a solution of 500 mg (1.91 mmol) of 3-(5-chlorothiophene-2-carbonyl)oxazolidine-5-carboxylic acid and 367 mg (1.91 mmol) of 4-(4-aminophenyl)morpholin-3-one in 5 ml of dimethylformamide (DMF), and the mixture is stirred at room temperature for 18 hours. The reaction mixture is added to saturated sodium hydrogencarbonate solution, and the precipitate formed is filtered off, giving N-[4-(3-oxomorpholin-4-yl)phenyl]-3-(5-chlorothiophene-2-carbonyl)oxazolidine-5-carboxamide (“A5”) as a colourless solid; ESI 436.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906516B2
Source datasetuspto-grants-2011_03
ORD IDord-3b7c1de6f8e74a89bc56bd77208a609d
Source noteuspto-grants-2011_03