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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515813Generated: October 29, 2026

Methyl p-toluenesulfonate → HCID 86683472, compound

https://huagongshe.com/reaction/515813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantCesium carbonateHCID 10796—
ReactantHCID 86683473HCID 86683473—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 86683472HCID 8668347230.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 4-(7-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-8-oxo-6-thioxo-5,7-diazaspiro-[3.4]octan-5-yl)benzenesulfonamide (Compound 81, 97 mg, 0.20 mmol), methyl tosylate (37 mg, 0.20 mmol), and Cs2CO3 (65 mg, 0.20 mmol) in acetonitrile (1 mL) was heated at 50° C. for 20 h in a sealed tube. After being cooled room temperature, the reaction mixture was diluted with water and extracted with EtOAc (3×). The organic layer was dried over magnesium sulfate and concentrated to give a residue that was purified by column chromatography on silica gel (hexanes:DCM:acetone=5:9:1) to afford 30 mg of 4-(7-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-8-oxo-6-thioxo-5,7-diazaspiro[3.4]-octan-5-yl)-N-methylbenzenesulfonamide as a white solid. 1H NMR (400 MHz, CDCl3) δ 9.11 (s, 1H), 8.37 (s, 1H), 8.10 (dd, 2H), 7.58-7.49 (m, 2H), 4.52 (d, 1H), 2.80 (m, 3H), 2.78-2.69 (m, 2H), 2.63-2.47 (m, 2H), 2.29 (m, 1H), 1.74 (m, 1H). LCMS [M+1+Na]+ 518.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108944B2
Source datasetuspto-grants-2015_08
ORD IDord-9a402d95914a480183c152dc533ae513
Source noteuspto-grants-2015_08