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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672743Generated: November 1, 2026

Sodium Carbonate → 3-(2,6-Dichloro-4-pyridin-3-yl-benzyl)-1-(4,4-difluoro-cyclohexyl)-pyrrolidin-2-one

https://huagongshe.com/reaction/1672743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantTrifluoro-methanesulfonic acid 3,5-dichloro-4-[1-(4,4-difluoro-cyclohexyl)-2-oxo-pyrrolidin-3-ylmethyl]-phenyl esterHCID 57878605—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product3-(2,6-Dichloro-4-pyridin-3-yl-benzyl)-1-(4,4-difluoro-cyclohexyl)-pyrrolidin-2-oneHCID 57878596—

Reaction Steps

Heat a solution of trifluoro-methanesulfonic acid 3,5-dichloro-4-[1-(4,4-difluoro-cyclohexyl)-2-oxo-pyrrolidin-3-ylmethyl]-phenyl ester (Preparation 33) (0.585 g, 1.15 mmol), pyridine-3-boronic acid (0.283 g, 2.30 mmol), Pd(PPh3)4 (133 mg), 11.5 mL of 0.1 M Na2CO3 aq solution in 11.5 mL of dimethoxy ethane at 80° C. for 24 hr. Cool the mixture to room temp and dilute with 20 mL of 1N NaHCO3. Dilute the mixture with 20 mL of EtOAc. Wash the organic layer with water, then brine, and dry over Na2SO4, filter and concentrate. Purify the crude material by chromatography to afford the title compound: mass spectrum (m/z): 439 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998999B2
Source datasetuspto-grants-2011_08
ORD IDord-02b3eaa3d155473c9c714eb6f08fdfd1
Source noteuspto-grants-2011_08