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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602322Generated: October 30, 2026

4-Methylmorpholine → HCID 11305076, compound

https://huagongshe.com/reaction/602322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant5-Chloro-2-thiophenecarboxylic acidHCID 95048—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 66593134HCID 66593134—
SolventDimethylformamideHCID 6228—
ProductHCID 11305076HCID 11305076—

Reaction Steps

0.71 g (4.66 mmol) of 1-hydroxybenzotriazole hydrate, 0.76 g (4.66 mmol) of 5-chlorothiophenecarboxylic acid, 1.79 g (9.33 mmol) of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (DAPECI) and 1.13 ml of N-methylmorpholine are added successively to a solution of 1.35 g (4.66 mmol) of N-[4-(3-oxomorpholin-4-yl)phenyl]pyrrolidine-2-carboxamide in 30 ml of dimethylformamide, and the resultant solution is stirred at room temperature for 12 hours. The reaction solution is subsequently evaporated to dryness under reduced pressure, the residue is taken up in 10 ml of 5% sodium hydrogencarbonate solution, and the sodium hydrogencarbonate solution is extracted twice with 10 ml of ethyl acetate each time. After the combined organic phases have been dried over sodium sulfate and the solvent has been stripped off, the solid residue is triturated with 20 ml of diethyl ether, giving 1.2 g (59.4%) of “AB1”, ESI 434; m.p. 195°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906516B2
Source datasetuspto-grants-2011_03
ORD IDord-0952af2cb0ee4f91974b13514b71cea9
Source noteuspto-grants-2011_03