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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528204Generated: November 4, 2026

C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine → HCID 71525796, compound

https://huagongshe.com/reaction/1528204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantC-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamineHCID 89525357—
ReactantHCID 89534499HCID 89534499—
SolventEthanolHCID 702—
ProductHCID 71525796HCID 7152579679%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 408.4 mg of methyl (R)-1-[3-(2-methoxy-3,4-dioxocyclobut-1-enylamino)benzenesulfonyl]pyrrolidine-2-carboxylate and 350 mg of C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine in 30 ml of ethanol was heated at 60° C. overnight. The solvent was evaporated off and the residue was taken up with 50 ml of ethyl acetate and washed twice with a 1 M sodium hydrogen phosphate solution. The organic phase was dried over magnesium sulfate and evaporated. 432 mg of methyl (R)-1-[3-(2-{[(5-methylfuran-2-yl)-(3-methyloxetan-3-yl)methyl]amino}-3,4-dioxocyclobut-1-enylamino)benzenesulfonyl]pyrrolidine-2-carboxylate were obtained. Yield=79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090596B2
Source datasetuspto-grants-2015_07
ORD IDord-d4bf8f1f89574a688389c44ba5c44aa7
Source noteuspto-grants-2015_07