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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080191Generated: October 30, 2026

Furfurylamine → 2-Amino-6-(furfurylamino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide

https://huagongshe.com/reaction/2080191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfurylamineHCID 3438—
ReactantA-101HCID 188218—
Reactant2-aminochloro-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamideHCID 23130498—
SolventDimethyl SulfoxideHCID 679—
SolventDiisopropylethylamineHCID 81531—
SolventSodium chloride; waterHCID 57417360—
Product2-Amino-6-(furfurylamino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamideHCID 2313059868%

Reaction Conditions

Temperature135 °C

Reaction Steps

2-Amino-6-chloro-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide described in Example A-101 (180 mg, 0.5 mmol) was dissolved in a mixture solution of dimethylsulfoxide (2 mL) and diisopropylethylamine (1 mL), furfurylamine (0.663 mL, 7.5 mmol) was added, and the solution was heated in a sealed tube for 13 hours 30 minutes (oil bath temperature: 135° C.). The reaction mixture was allowed to room temperature, poured into brine, and the solution was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, then concentrated, the obtained residue was purified by NH silica gel column chromatography (ethyl acetate:hexane=2:1), and the title compound (144 mg, 0.34 mmol, 68%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-08831688426e44ab9c30259721c4a998
Source noteuspto-grants-2011_04