Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079974Generated: October 30, 2026

2-Aminonicotinic acid → 2-amino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide

https://huagongshe.com/reaction/2079974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminonicotinic acidHCID 72930—
ReactantC-(5-Phenoxy thiophen-2-yl)methylamineHCID 23130515—
Product2-amino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamideHCID 23130423—

Reaction Steps

2-Amino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide (250 mg, 0.768 mmol) obtained from 2-aminonicotinic acid and C-(5-phenoxy-thiophen-2-yl)methylamine described in Preparation Example 24 according to an analogous method to Preparation Example A+-5, and N-iodosuccinimide (190 mg, 0.845 mmol) were dissolved in tetrahydrofuran (5 mL), and the solution was stirred for 16 hours at room temperature. An aqueous solution of saturated sodium bicarbonate was added to the reaction solution at 0° C., which was then extracted with ethyl acetate, the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated in vacuo, residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=1:1), and title compound (45 mg, 0.10 mmol, 13%) was obtained as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-e5540f853ea64e34b09f5c4e1a094638
Source noteuspto-grants-2011_04