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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386902Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 45111497, compound

https://huagongshe.com/reaction/386902

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 59253165HCID 59253165—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 45111497HCID 45111497100%

Reaction Steps

A solution of 192 mg (0.35 mmol) of 2-(1-methanesulfonylpiperidine-4-sulfonyl)-2-methyl-N-{3-[(3S)-2-methyl-3-(oxan-2-yloxy)butan-2-yl]-1,2-oxazol-5-yl}propanamide in DCM/methanol (1/1, 4 mL) is treated with 241 mg (1.40 mmol) of MP-TsOH resin (loading 3.3 mmol/g) at room temperature for 18 h. The resin is removed by filtration and washed alternating with DCM and methanol. The combined filtrates are concentrated under reduced pressure and the resulting residue is purified by column chromatography (silica, eluent: heptanes, 50-100% ethyl acetate) to yield 163 mg of N-{3-[(3S)-3-hydroxy-2-methylbutan-2-yl]-1,2-oxazol-5-yl}-2-(1-methanesulfonylpiperidine-4-sulfonyl)-2-methylpropanamide. Yield 78%; ES-MS: m/z 466 [M+H]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372874B2
Source datasetuspto-grants-2013_02
ORD IDord-5a3d265b1f9e498face759708be67632
Source noteuspto-grants-2013_02