HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634213Generated: November 1, 2026
Potassium Hydroxide → HCID 86758788, compound
https://huagongshe.com/reaction/1634213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Bromofuran-2-carbaldehyde | HCID 600328 | — |
| Reactant | O-mesitylenesulfonylhydroxylamine | HCID 11009332 | — |
| Reactant | HCID 86758787 | HCID 86758787 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86758788 | HCID 86758788 | 21% |
Reaction Steps
To a solution of 39 mg (0.17 mmol) cyclopentanecarboxylic acid (2,6-diamino-pyridin-4-ylmethyl)-amide in 1.4 ml dioxane was added 40.2 mg (0.187 mmol, 1.1 eq.) o-mesitylenesulfonylhydroxylamine and after 2h 38.6 mg (0.221 mmol, 1.3 eq.) 5-bromo-2-furaldehyde. The mixture was heated to 100° C. for 2.5 h and afterwards 0.17 ml 1N KOH in MeOH was added. Opening of the reaction vessel and stirring of the mixture at room temperature for 16 h preceded the evaporation to dryness. The residue was taken up in 4.5 ml water and the aqueous phase was extracted with dichloromethane. The combined organic layers were dried with MgSO4 and evaporated. Purification of the residue with column chromatography on silica eluting with yielded the 12 mg (21%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06506772B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-52d48d653c7f494c8dfdcf5982e9271d |
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| Source note | uspto-grants-2003_01 |
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