HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050414Generated: November 1, 2026
Methanesulfonic Acid → HCID 118598606, compound
https://huagongshe.com/reaction/1050414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 118598780 | HCID 118598780 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 118598606 | HCID 118598606 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382248B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-39aadc5108d14d31abed4c5ee85c248a |
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| Source note | uspto-grants-2016_07 |
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