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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433817Generated: October 30, 2026

HCID 20610247, compound → HCID 20610318, compound

https://huagongshe.com/reaction/433817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20610247HCID 20610247—
ReactantHCID 20610270HCID 20610270—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20610318HCID 2061031856%

Reaction Conditions

Temperature125 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06668527B2
Source datasetuspto-grants-2003_12
ORD IDord-5c76c4a7daf5438cab96058325b857ae
Source noteuspto-grants-2003_12