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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676519Generated: October 26, 2026

Triethylamine → 4-amino-N-(1-ethyl-4-piperidyl)-3-methoxy-benzamide

https://huagongshe.com/reaction/1676519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethylpiperidin-4-amineHCID 3734990—
Reactant4-Amino-3-methoxy-benzoic acid benzotriazol-1-yl esterHCID 10660685—
SolventTetrahydrofuranHCID 8028—
Product4-amino-N-(1-ethyl-4-piperidyl)-3-methoxy-benzamideHCID 5801509390.6%

Reaction Steps

To a mixture of 1.1371 g (4.0 mmole) of 4-amino-3-methoxy-benzoic acid benzotriazol-1-yl ester and 8 mL of dry tetrahydrofuran at 0 degrees was added 0.5129 g (4.0 mmole) of 4-amino-1-ethylpiperidine followed by 1.0119 g (10 mmole) of triethylamine. The cooling bath was removed and the mixture stirred at room temperature for 65 minutes. Volatiles were removed under reduced pressure and the residue taken up in ethyl acetate, and the organic layer washed twice with 50 mL of 0.5 M sodium carbonate, 50 mL water, and then 50 mL brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 1.0056 g 4-amino-N-(1-ethyl-piperidin-4-yl)-3-methoxy-benzamide, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003785B2
Source datasetuspto-grants-2011_08
ORD IDord-357262a32ce5484996c6b5631562f8a2
Source noteuspto-grants-2011_08