HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528183Generated: November 2, 2026
HCID 58736381, compound → HCID 71525424, compound
https://huagongshe.com/reaction/1528183
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58736381 | HCID 58736381 | — |
| Reactant | C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine | HCID 89525357 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71525424 | HCID 71525424 | 70.1% |
Reaction Steps
A mixture of 284 mg (0.87 mmol, 1 eq) of 2-hydroxy-3-(2-methoxy-3,4-dioxocyclobut-1-enylamino)-N,N-dimethylbenzenesulfonamide and 318 mg (1.75 mmol) of C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine in 20 ml of methanol was heated at 50° C. for 3 days. The reaction medium was concentrated. The residue was taken up in ethyl acetate and was washed twice with a 1 M aqueous sodium dihydrogen phosphate solution. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. 0.29 g of product was obtained in the form of an ochre solid. Yield=70%, HPLC=98.68%, Mp=123° C.
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-54e8a16d5c28489f8b356f14ac3217ab |
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| Source note | uspto-grants-2015_07 |
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