HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433660Generated: October 30, 2026
HCID 20610247, compound → HCID 20610318, compound
https://huagongshe.com/reaction/433660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20610247 | HCID 20610247 | — |
| Reactant | HCID 20610270 | HCID 20610270 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20610318 | HCID 20610318 | 56% |
Reaction Steps
A mixture of 2-allyloxycarbonylamino-2-[3-(1-tert-butoxycarbonyl-pyrrolidin-2-yl)-isoxazol-5-ylmethyl]-malonic acid monoethyl ester and 2-allyloxycarbonylamino-2-[3-(1-tert-butoxycarbonyl-pyrrolidin-2-yl)-isoxazol-5-ylmethyl]-malonic acid diethyl ester (10.4 g, 21.5 mmol) was dissolved in dioxane (130 mL) and heated in an oil bath to 125° C. for 3 hours. The dioxane was then removed in vacuo. The residue was dissolved in ethyl acetate, washed with saturated sodium carbonate and brine, dried over magnesium sulfate and concentrated. The crude material was chromatographed on a Biotage Flash 40M column eluting with ethyl acetate/hexanes (1:4) to give the title compound as a clear oil (5.12 g, 56% 2 steps). MS (CI) m/z 338.0 (M-99). 2-Allyloxycarbonylamino-2-[3-(1-tert-butoxycarbonyl-pyrrolidin-2-yl)isoxazol-5-ylmethyl]-malonic acid diethyl ester was recovered (2.96 g, 27%). MS (CI) m/z 509.9 (M+1), 409.9 (M-99)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06667331B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-3d3e4b6173784da49f1f709530af282a |
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| Source note | uspto-grants-2003_12 |
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