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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028147Generated: October 30, 2026

Ethyl 1-[4-(3-nitrophenyl)-1,3-thiazol-2-yl]piperidine-4-carboxylate → Ethyl 1-[4-(3-aminophenyl)-1,3-thiazol-2-yl]piperidine-4-carboxylate

https://huagongshe.com/reaction/1028147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-[4-(3-nitrophenyl)-1,3-thiazol-2-yl]piperidine-4-carboxylateHCID 71075037—
CatalystPalladiumHCID 23938—
ProductEthyl 1-[4-(3-aminophenyl)-1,3-thiazol-2-yl]piperidine-4-carboxylateHCID 7723105660%

Reaction Steps

To a solution of the ethyl 1-[4-(3-nitrophenyl)-1,3-thiazol-2-yl]piperidine-4-carboxylate (457 mg, 1.26 mmol) in ethyl acetae (10 mL) and acetic acetic acid (1 mL) was added 10% palladium on carbon (135 mg, 0.126 mmol) and the mixture was placed under an atmosphere of H2 (balloon). The mixture was stirred for 3 hours was then filtered through celite. The filtrate was concentrated under reduced pressure. The resulting residue was purified by CombiFlash (20-60% ethyl acetate:hexanes) provided 250 mg (0.754 mmol, 60% yield) of ethyl 1-[4-(3-aminophenyl)-1,3-thiazol-2-yl]piperidine-4-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735417B2
Source datasetuspto-grants-2014_05
ORD IDord-106900a4a2b940e4a01ce58cf73acda3
Source noteuspto-grants-2014_05