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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303803Generated: November 3, 2026

Triethylamine → HCID 18461302, compound

https://huagongshe.com/reaction/2303803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(4-((2,4-Dioxothiazolidin-5-YL)methyl)phenoxy)acetic acidHCID 11323485—
ReactantHCID 18461450HCID 18461450—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18461302HCID 18461302—

Reaction Steps

A mixture of t-butyl N-[2-amino-5-(4′-hydroxybiphenyl-1-yloxy)phenyl]-N-methylcarbamate (0.61 g), 4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxyacetic acid (0.51 g), diethyl cyanophsphonate (0.29 g), triethylamine (0.18 g) and anhydrous tetrahydrofuran (10 ml) was stirred at ambient temperature for 2 days. The reaction mixture was concentrated and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was dried over anhydrous sodium sulfate. The ethyl acetate was distilled off under reduced pressure and the residue was purified by chromatography on a silica gel column using n-hexane/ethyl acetate=1/1 as the eluant to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432993B1
Source datasetuspto-grants-2002_08
ORD IDord-1e9fd8a4195144bb8dcb192bfd2ccaf6
Source noteuspto-grants-2002_08