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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620295Generated: October 29, 2026

HCID 13799295, compound → HCID 178466800, compound

https://huagongshe.com/reaction/620295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13799295HCID 13799295—
SolventTrifluoroacetic acidHCID 6422—
SolventAnisoleHCID 7519—
ProductHCID 178466800HCID 178466800—

Reaction Steps

A solution of 3 g (4.5 mmol) of N-{{3-{3-[4-acetyl-3-hydroxy-2-(3,3,3-trifluoropropyl)-phenoxy]-propoxy}-4-chloro-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}-4-chloro-6-methyl-phenyl}}-1H-tetrazole-5-carboxamide thus obtained, of melting point 236°-238° (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, crystallisation starts. The sodium salt of N-{{3-{3-[4-acetyl-3-hydroxy-2-(3,3,3-trifluoropropyl)-phenoxy]-propoxy}-4-chloro-6-methylphenyl}}-1 H-tetrazole-5-carboxamide of melting point 90° (decomposition) is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820726
Source datasetuspto-grants-1989_04
ORD IDord-e691b51619f04fc39bd86e12b8110863
Source noteuspto-grants-1989_04