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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691868Generated: November 2, 2026

Triethylamine → HCID 57652009, compound

https://huagongshe.com/reaction/1691868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-5-nitropyridineHCID 78240—
Reactant4-N-Boc-4-N-Methyl-aminopiperidineHCID 2756806—
SolventDimethylformamideHCID 6228—
ProductHCID 57652009HCID 5765200985.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-bromo-5-nitro-pyridine (4.74 g, 23.3 mmol), methyl-piperidin-4-yl-carbamic acid tert-butyl ester (5 g, 23.3 mmol), and triethylamine (5 mL) in N,N-dimethylformamide (30 mL) was stirred at 90° C. for 14 h. Upon completion of the reaction, the reaction mixture was partitioned between water and ethyl acetate. The aqueous layer was extracted with ethyl acetate twice. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue was recrystallized from methanol and water to give methyl (5′-nitro-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl)-carbamic acid tert-butyl ester (6.7 g, 85.5%) as brown crystals. LCMS calcd for C16H24N4O4 (m/e) 336, obsd 337 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153644B2
Source datasetuspto-grants-2012_04
ORD IDord-2e00029f888249f0adbd3d500347844a
Source noteuspto-grants-2012_04