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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456015Generated: October 29, 2026

Methanesulfonic Acid → HCID 178424629, compound

https://huagongshe.com/reaction/456015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 178424627HCID 178424627—
SolventEthanolHCID 702—
ProductHCID 178424629HCID 17842462940%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497376B2
Source datasetuspto-grants-2013_07
ORD IDord-41ef2368dd194b7bb15efe1528504f20
Source noteuspto-grants-2013_07