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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595866Generated: October 31, 2026

Sodium methanethiolate → HCID 118049844, compound

https://huagongshe.com/reaction/595866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
ReactantHCID 118051738HCID 118051738—
SolventMethanolHCID 887—
ProductHCID 118049844HCID 118049844108.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of (+/−)-(1S,3R)-3-(6-(4-(benzylcarbamoyl)-3-fluorophenyl)-5-pivalamidopyrazin-2-yl)cyclohexyl methanesulfonate (25 mg, 0.043 mmol) and sodium methanethiolate (24.09 mg, 0.344 mmol) in MeOH (430 μL) was heated at 80° C. for 2 h. Solvent was removed and the residue was purified with flash chromatography eluting with EtOAc (containing 10% of MeOH)/heptane to provide 25 mg of crude (+/−)-N-benzyl-2-fluoro-4-(6-((1R,3R)-3-(methylthio)cyclohexyl)-3-pivalamidopyrazin-2-yl)benzamide which was taken to the next step without further purification. LCMS (m/z): 535.3 (MH+), 1.09 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-56fb5343307048e0a26f101e0e7492f6
Source noteuspto-grants-2016_01