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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2575Generated: October 27, 2026

Diphenylmethyl aminoxy-[3-fluoro-4,5-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-acetate → [[[1-[3-Fluoro-4,5-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-2-oxo-2-(diphenylmethoxy)-ethyl]-oxy]-imino]-[2-[(triphenylmethyl)-amino]-thiazol-4-yl]-acetic acid

https://huagongshe.com/reaction/2575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylmethyl aminoxy-[3-fluoro-4,5-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-acetateHCID 9829251—
Reactant(2-Triphenylmethylamino-4-thiazolyl)glyoxylic acidHCID 11133448—
SolventMethanolHCID 887—
Product[[[1-[3-Fluoro-4,5-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-2-oxo-2-(diphenylmethoxy)-ethyl]-oxy]-imino]-[2-[(triphenylmethyl)-amino]-thiazol-4-yl]-acetic acidHCID 8505340756%

Reaction Steps

0.640 g of the product of Step D and and 0.474 g of oxo-[2-[(triphenylmethyl)-amino]-thiazol-4-yl]-acetic acid (Belgian Patent Application No. 864,828) were stirred for 4 and a half hours under nitrogen and at ambient temperature in the presence of 20 ml of methanol. Then, the solvent was eliminated, and the residue was chromatographed on silica, eluting with a dichloromethane-methanol (95-5) mixture to obtain 0.612 g of the expected product with a Rf=0.35 [eluant: dichloromethane-methanol (9-1)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728828
Source datasetuspto-grants-1998_03
ORD IDord-0a483aea8a4b498cbaefafb7e4383a84
Source noteuspto-grants-1998_03