Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515121Generated: October 25, 2026

4-Methyl-5-((2R)-oxiran-2-yl)-2-benzofuran-1(3H)-one → 6-(1-Hydroxy-2-((R)-3-((R)-2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)ethylamino)pyrrolidin-1-yl)ethyl)nicotinonitrile

https://huagongshe.com/reaction/515121

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-5-((2R)-oxiran-2-yl)-2-benzofuran-1(3H)-oneHCID 59568646—
Reactant6-{2-[(3R)-3-aminopyrrolidin-1-yl]-1-hydroxyethyl}pyridine-3-carbonitrile hydrochlorideHCID 90410632—
Product6-(1-Hydroxy-2-((R)-3-((R)-2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)ethylamino)pyrrolidin-1-yl)ethyl)nicotinonitrileHCID 71565791—

Reaction Steps

6-(1-Hydroxy-2-((R)-3-((R)-2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)ethylamino)pyrrolidin-1-yl)ethyl)nicotinonitrile was prepared in a similar fashion to that described for the synthesis of EXAMPLE 1 starting from 6-{2-[(3R)-3-aminopyrrolidin-1-yl]-1-hydroxyethyl}pyridine-3-carbonitrile hydrochloride [INTERMEDIATE 11] and 4-methyl-5-[(2R)-oxiran-2-yl]-2-benzofuran-1(3H)-one [INTERMEDIATE 2B].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108947B2
Source datasetuspto-grants-2015_08
ORD IDord-c98eaa3b73b34a0f962e04403fca1ddb
Source noteuspto-grants-2015_08