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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528186Generated: October 29, 2026

C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine → HCID 178425500, compound

https://huagongshe.com/reaction/1528186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantC-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamineHCID 89525357—
ReactantHCID 178493669HCID 178493669—
SolventMethanolHCID 887—
ProductHCID 178425500HCID 17842550043.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 263 mg (1.45 mmol, 1.2 eq) of C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine and 1.02 g (1.21 mmol, 1 eq) of 3-(3H-benzotriazol-4-ylamino)-4-methoxycyclobut-3-ene-1,2-dione at 29% in 25 ml of methanol was heated at 50° C. for 24 hours. The insoluble material (dimer) was filtered off and the filtrate was evaporated. The residue was chromatographed on silica gel (column puriFlash PF-30SIHP/40G, Spot II) eluted with dichloromethane/methanol (gradient). The solid was taken up with ethyl acetate and this organic phase was washed several times with a 1 N sodium dihydrogen phosphate solution, dried over magnesium sulfate, filtered and evaporated. 205 mg of 3-(3H-benzotriazol-4-ylamino)-4-{[(5-methyl furan-2-yl)-(3-methyloxetan-3-yl)methyl]amino}cyclobut-3-ene-1,2-dione were obtained in the form of a yellow solid. (Mp=178-180° C.). Yield=43%, LC/MS: 95.97% [393].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090596B2
Source datasetuspto-grants-2015_07
ORD IDord-0feb7e392efd40f3b32246fcfe036548
Source noteuspto-grants-2015_07