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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807111Generated: October 31, 2026

Pyridinium.p-toluenesulfonate → HCID 86640470, compound

https://huagongshe.com/reaction/1807111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium.p-toluenesulfonateHCID 22033616—
ReactantHCID 86640469HCID 86640469—
SolventMethanolHCID 887—
ProductHCID 86640470HCID 86640470—

Reaction Steps

A mixture of rac-(2R,3R,4R,5S)-3-(3-chloro-phenyl)-4-(4-chloro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carboxylic acid [1-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-1H-pyrazol-3-yl]-amide (81 mg, 0.133 mmol), pyridinium p-toluene sulfonic acid (5 mg, 0.0198 mmol) and methanol (4 mL) was microwaved at 120° C. for 5 min. Solvent evaporated and purified by reverse phase chromatography (20-95% of ACN/water) to rac-(2R,3R,4R,5S)-3-(3-chloro-phenyl)-4-(4-chloro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carboxylic acid [1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-amide (26.5 mg, 35%) as an off-white powder. HRMS (ES+) m/z Calcd for C29H33Cl2N5O3S+H [(M+H)+]: 570.2033. found: 570.2032.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-c0d41e446c9b498ca21c2ca5a0cf24d8
Source noteuspto-grants-2013_01