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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050414Generated: November 1, 2026

Methanesulfonic Acid → HCID 118598606, compound

https://huagongshe.com/reaction/1050414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 118598780HCID 118598780—
SolventChloroformHCID 6212—
ProductHCID 118598606HCID 118598606—

Reaction Conditions

Temperature50 °C

Reaction Steps

6′-((4-Methoxybenzyl)thio)-8′-methyl-2′H-spiro[cyclohexane-1,3′-imidazo[1,5-c]pyridine]-1′,5′-dione (3, 3.3 g, 8.59 mmol) was dissolved in chloroform (20 mL) and methanesulfonic acid (10 mL) was added. The reaction mixture was stirred at 50° C. for 16 h. After completion, solvent was evaporated under reduced pressure. Obtained crude was washed with water (50 mL) followed by ethyl acetate and then dried under reduced pressure to afford 6′-mercapto-8′-methyl-2′H-spiro[cyclohexane-1,3′-imidazo[1,5-a]pyridine]-1′,5′-dione as grey solid. Yield: 1.3 g, 59%; MS (ESI) m/z 265.6 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382248B2
Source datasetuspto-grants-2016_07
ORD IDord-39aadc5108d14d31abed4c5ee85c248a
Source noteuspto-grants-2016_07