HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456015Generated: October 29, 2026
Methanesulfonic Acid → HCID 178424629, compound
https://huagongshe.com/reaction/456015
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 178424627 | HCID 178424627 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178424629 | HCID 178424629 | 40% |
Reaction Steps
A solution of 4-cyano-1H-imidazole-2-carboxylic acid[2-(4,4-dimethyl-cyclohex-1-enyl)-6-(2,2,6,6-tetramethyl-tetrahydro-pyran-4-yl)-pyridin-3-yl]-amide (50.0 mg, 0.108 mmol, as prepared in Example 15, step (h)) in EtOH (2 mL) was treated with methanesulfonic acid (7.0 μL, 0.108 mmol) at room temperature for 1 h. The solvents were evaporated in vacuo, and the residue was dried under high vacuum overnight. The solid was dissolved in a minimum amount of EtOH (2 mL) with sonication and heating. While warm, the solution was slowly treated with hexanes (3 mL) to the cloud point. The mixture was heated again until clear, the sides of the vial were scratched, and the mixture was allowed to cool. The solid was filtered and air-dried to afford the title compound (24 mg, 40%) as white crystals. Mass spectrum (APCI, m/z): Calcd. for C27H35N5O2, 462.3 (M+H), found 462.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497376B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-41ef2368dd194b7bb15efe1528504f20 |
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| Source note | uspto-grants-2013_07 |
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