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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643707Generated: October 30, 2026

p-Toluenesulfonic acid monohydrate → HCID 68615352, compound

https://huagongshe.com/reaction/643707

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantN-(5-Bromo-2-{[(1-hydroxycyclopentyl)methyl]amino}phenyl)-2,2-dimethylpropanamideHCID 68614758—
SolventTolueneHCID 1140—
ProductHCID 68615352HCID 6861535238%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of N-(5-bromo-2-{[(1-hydroxycyclopentyl)methyl]amino}phenyl)-2,2-dimethylpropanamide (Step C, 1.3 g, 3.41 mmol) in toluene (100 mL) was added p-toluenesulfonic acid monohydrate (130 mg, 0.68 mmol) at room temperature and the mixture was stirred at 140° C. for 23 h. After cooling to room temperature, p-toluenesulfonic acid monohydrate (130 mg, 0.68 mmol) was added, and the mixture was heated at 140° C. After stirring for 26 h at 140° C., the mixture was quenched with saturated sodium hydrogen carbonate aqueous solution. The mixture was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate:dichloromethane=5.5:1:0.5 as eluent) to afford the title compound (453 mg, 38%) as a beige amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700618B2
Source datasetuspto-grants-2010_04
ORD IDord-65e5ac6b6b0a4a13a3d244dc16f0e236
Source noteuspto-grants-2010_04