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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509585Generated: November 1, 2026

Tosylmethyl isocyanide → HCID 58355311, compound

https://huagongshe.com/reaction/1509585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTosylmethyl isocyanideHCID 161915—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 58355275HCID 58355275—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 58355311HCID 5835531139.2%

Reaction Steps

tert-Butyl (3S,5R)-3-[{[1-(2-fluorophenyl)-5-(4-methoxybutyl)-1H-1,2,3-triazol-4-yl]carbonyl}(2-methylpropyl)amino]-5-formylpiperidine-1-carboxylate (235 mg) and tosylmethyl isocyanide (125 mg) were dissolved in methanol (4 ml), sodium methoxide (28% methanol solution, 325 mg) was added and the mixture was heated under reflux with stirring for 2 hr. The mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (5:95-100:0) was concentrated under reduced pressure to give the object product (98.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221836B2
Source datasetuspto-grants-2015_12
ORD IDord-aecacfd8ec7d48ec9b8319e433b4d1fb
Source noteuspto-grants-2015_12