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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080212Generated: November 2, 2026

Water → 2-Methylamino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide

https://huagongshe.com/reaction/2080212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(Ethoxymethyl-amino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamideHCID 23130432—
SolventDimethyl SulfoxideHCID 679—
Product2-Methylamino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamideHCID 2313069667%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-(ethoxymethyl-amino)-N-(5-phenoxy-thiophene-2-ylmethyl)-nicotinamide described in Preparation Example A+-6 (148 mg, 0.385 mmol) in dimethylsulfoxide (3 mL) was added sodium borohydride (44 mg, 1.15 mmol), and the solution was stirred for 30 minutes at 100° C., followed by stirring for 20 minutes at 110° C. Furthermore, sodium borohydride (35 mg, 0.925 mmol) was added thereto, followed by stirring for 20 minutes at 110° C. Water was added to the reaction mixture, which was then extracted with ethyl acetate, the organic layer was sequentially washed with water and brine, dried over anhydrous sodium sulfate, and then, concentrated in vacuo. The obtained residue was purified by silica gel chromatography (hexane-ethyl acetate), and the title compound (86 mg, 0.26 mmol, 67%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-678f674f3e75494cb9068c34d2c9f122
Source noteuspto-grants-2011_04