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
Participants
| Role | Name | HCID | Charge |
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| Reactant | C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine | HCID 89525357 | — |
| Reactant | HCID 89534499 | HCID 89534499 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 71525796 | HCID 71525796 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090596B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-d4bf8f1f89574a688389c44ba5c44aa7 |
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| Source note | uspto-grants-2015_07 |
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