HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086913Generated: October 28, 2026
HCID 13799295, compound → HCID 178466800, compound
https://huagongshe.com/reaction/1086913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 13799295 | HCID 13799295 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 178466800 | HCID 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 9020 (decomposition) is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05032606 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-dd27899cd04b47de84500f149facd545 |
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| Source note | uspto-grants-1991_07 |
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