Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382815Generated: November 1, 2026

HCID 15718333, compound → HCID 178439719, compound

https://huagongshe.com/reaction/1382815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15718333HCID 15718333—
SolventTrifluoroacetic acidHCID 6422—
SolventAnisoleHCID 7519—
ProductHCID 178439719HCID 178439719—

Reaction Steps

A solution of 7.1 g (11.8 mmol) of N-{3-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-2-hydroxypropoxy]-2-cyanophenyl}-1-(4-methoxybenzyl)tetrazole-5-carboxamide in 150 ml of trifluoroacetic acid and 15 ml of anisole is heated at reflux temperature for 30 minutes. The reaction mixture is concentrated under reduced pressure, about 200 ml of ether and 300 ml of petroleum ether are added to the residue, and the crystals are filtered off. The N-{3-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-2-hydroxypropoxy]-2-cyanophenyl}-1H-tetrazole-5-carboxamide of melting point 210°-213° thus obtained is dissolved in 50 ml of hot acetone, and one equivalent of triethanolamine in 20 ml of acetone is added. Crystallisation sets in after ether has been addded. This gives the triethanolammonium salt of N-{3-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-2-hydroxypropoxy]-2-cyanophenyl}-1H-tetrazole-5-carboxamide of melting point 80°-82°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808604
Source datasetuspto-grants-1989_02
ORD IDord-ae2968378bff449cbc60d00a75e8b80a
Source noteuspto-grants-1989_02