Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086936Generated: October 31, 2026

HCID 19818603, compound → HCID 178466798, compound

https://huagongshe.com/reaction/1086936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19818603HCID 19818603—
SolventTrifluoroacetic acidHCID 6422—
SolventAnisoleHCID 7519—
ProductHCID 178466798HCID 178466798—

Reaction Steps

A solution of 2.84 g (4.5 mmol) of N-{{3-{3-[4-acetyl-3-hydroxy-2-(3,3,3-trifluoropropyl)-phenoxy]-propoxy}-6-methyl-phenyl}}-1-(4-methoxybenzyl)-tetrazole-5-carboxamide in 90 ml of trifluoroacetic acid and 9 ml of anisole is refluxed for 60 minutes. The reaction mixture is concentrated under reduced pressure, about 150 ml of ether and 300 ml of petroleum ether are added and the crystals are filtered off. The N-{{3-{3-[4-acetyl-3-hydroxy-2-(3,3,3-trifluoropropyl)-phenoxy]-propoxy}-6-methyl-phenyl}}-1H-tetrazole-5-carboxamide thus obtained, of melting point 236°-238° C. (decomposition), is dissolved in 50 ml of tetrahydrofuran, and one equivalent of sodium, dissolved in 5 ml of methanol, is added. After addition of ether, crystallizations starts. The sodium salt of N-{{3-{3-[4-acetyl-3-hydroxy-2-(3,3,3-trifluoropropyl)-phenoxy]-propoxy}-6-methyl-phenyl}}-1H-tetrazole-5-carboxamide of melting point 115°-125° C. (decomposition) is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05032606
Source datasetuspto-grants-1991_07
ORD IDord-e8db2378b5c34b1f91a2ba1fc1417a2c
Source noteuspto-grants-1991_07