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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159229Generated: November 2, 2026

Water → 5-(4-Chloro-phenyl)-N-((R)-1-hydroxymethyl-3-methyl-butyl)-6-(2-propionylamino-ethoxy)-nicotinamide

https://huagongshe.com/reaction/1159229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
ReactantSodium BicarbonateHCID 516892—
ReactantN-{2-[3-(4-Chloro-phenyl)-5-((R)-4-isobutyl-2,2-dimethyl-oxazolidine-3-carbonyl)-pyridin-2-yloxy]-ethyl}-propionamideHCID 67505397—
SolventMethanolHCID 887—
Product5-(4-Chloro-phenyl)-N-((R)-1-hydroxymethyl-3-methyl-butyl)-6-(2-propionylamino-ethoxy)-nicotinamideHCID 2485725176.7%

Reaction Steps

N-{2-[3-(4-Chloro-phenyl)-5-((R)-4-isobutyl-2,2-dimethyl-oxazolidine-3-carbonyl)-pyridin-2-yloxy]-ethyl}-propionamide (82 mg, 0.16 mmol) was dissolved in methanol (0.35 mL). To the solution was added camphorsulfonic acid (1.6 mg, 0.007 mmol) and the reaction mixture was stirred for 1 h at RT. The mixture was poured into water, sodiumbicarbonate was added and the mixture extracted with ethyl acetate. Organic phases were pooled, the solvent was evaporated in vacuo and the residue was purified by column chromatography on silica (dichloromethane/methanol gradient) to yield 55 mg of the title compound as a white solid, MS (ISP) 448.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812028B2
Source datasetuspto-grants-2010_10
ORD IDord-13a127b922fe4c28a3c938d2374372ff
Source noteuspto-grants-2010_10