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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464397Generated: October 29, 2026

1,4-Dioxane → HCID 178484876, compound

https://huagongshe.com/reaction/464397

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantL-Phenylalanine, methyl esterHCID 736234—
Reactant(2Z)-2-(2-oxopyrrolidin-3-yl)oxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acidHCID 13335553—
SolventMethanolHCID 887—
ProductHCID 178484876HCID 178484876—

Reaction Conditions

Temperature50 °C

Reaction Steps

30 g of (Z)-2-(2-tritylaminothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetic acid and 60 ml of methanol are added to 100 ml of dioxane containing 0.5 g of methyl L-phenylalaninate, and the mixture is heated at 50° C. to dissolve said acid therein. 700 ml of dioxane are added to the solution, and the mixture is stirred at room temperature for 5 hours. Crystalline precipitates are collected by filtration (the filtrate is hereinafter referred to as "Filtrate I"), and 14.3 g of the crude product thus obtained are dissolved in 24 ml of methanol. 280 ml of dioxane are added to the methanol solution. The mixture is stirred at room temperature for 4 hours, and crystalline precipitates are collected by filtration (the filtrate is hereinafter referred to as "Filtrate II"). 12.2 g of (Z)-2-(2-tritylaminothiazol-4-yl)-2-[((3S)-2-pyrrolidon-3-yl)oxyimino]acetic acid methyl L-phenylalaninate salt are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547494
Source datasetuspto-grants-1985_10
ORD IDord-e73121a1c5124337a6374f6f626d0f7e
Source noteuspto-grants-1985_10