US3947412A
Expired / Lapsed
US
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Process for the manufacture of 2-aryl-vic-triazoles
Assignee: Bayer AG
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Filing: 1973-11-06
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Granted: 1976-03-30
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Expires: 1993-11-06
Abstract
Abstract Vic-triazoles are obtained in almost quantitative yield and high purity when α-oximino-arylhydrazones of the formula ##EQU1## IN WHICH Ar represents an aromatic-carbocyclic or aromatic heterocyclic radical, R 1 denotes an aliphatic or aromatic radical, R 2 denotes hydrogen or an aliphatic or aromatic radical and n denotes the numbers 1 or 2, are reacted with at least 1 mol equivalent of a cyclising agent in the presence of heavy metals or of their ions.
Inventors
- 👤 Uwe Claussen
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-09 03:20
CPC Classifications
C; C07; C07D; C07D249/00; C07D249/02; C07D249/04
Claims Analysis
Total Claims: 4
Claim 1
Independent Claim
229 words
Process for the manufacture of 2-aryl-vic-triazoles which comprises reacting in the presence of copper or an ion of copper an α-oximino-arylhydrazone with a cyclizing agent wherein said aryl is a radical of the benzene, naphthalene, diphenyl, diphenylmethane, diphenylethane, stilbene, tolane, pyridine, triazole, imidazole, pyrazole, coumarin or carbostyril series and said cyclizing agent is selected from the group consisting of: a. acid anhydride of the formula ##EQU6## wherein R 3 and R 4 , independently of each other are C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, or phenyl; b. isocyanate of the formula R.sub.5 -N=C=O wherein R 5 is hydrogen, C 1 -C 6 -alkyl, C 5 -C 7 -cycloalkyl, phenyl, phenylcarbonyl, phenylsulphonyl, C 1 -C 6 -alkyl substituted by C 1 -C 4 -alkoxy, or phenyl substituted by C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, or nitro; c. acyl halide of the formula ##EQU7## wherein R 6 is C 1 -C 6 -alkyl, phenyl, C 1 -C 6 -alkylamino, phenylamino, substituted phenyl, where the substituent is C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, or halogen; d. urea of the formula ##EQU8## wherein R 7 , R 8 , and R 9 , independently of each other are hydrogen, C 1 -C 4 -alkyl, or phenyl; e. alkali metal salts of cyanic acid; and f. alkali metal salts of isocyanic acid.
Claim 2
Dependent Claim
229 words
Process for the manufacture of 2-aryl-vic-triazoles which comprises reacting in the presence of copper or an ion of copper an α-oximino-arylhydrazone with a cyclizing agent wherein said aryl is a radical of the benzene, naphthalene, diphenyl, diphenylmethane, diphenylethane, stilbene, tolane, pyridine, triazole, imidazole, pyrazole, coumarin or carbostyril series and said cyclizing agent is selected from the group consisting of: a. acid anhydride of the formula ##EQU6## wherein R 3 and R 4 , independently of each other are C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, or phenyl; b. isocyanate of the formula R.sub.5 -N=C=O wherein R 5 is hydrogen, C 1 -C 6 -alkyl, C 5 -C 7 -cycloalkyl, phenyl, phenylcarbonyl, phenylsulphonyl, C 1 -C 6 -alkyl substituted by C 1 -C 4 -alkoxy, or phenyl substituted by C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, or nitro; c. acyl halide of the formula ##EQU7## wherein R 6 is C 1 -C 6 -alkyl, phenyl, C 1 -C 6 -alkylamino, phenylamino, substituted phenyl, where the substituent is C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, or halogen; d. urea of the formula ##EQU8## wherein R 7 , R 8 , and R 9 , independently of each other are hydrogen, C 1 -C 4 -alkyl, or phenyl; e. alkali metal salts of cyanic acid; and f. alkali metal salts of isocyanic acid.
Claim 3
Dependent Claim
46 words
Process of claim 1 wherein said cyclizing agent is isocyanic acid, methyl isocyanate, ethyl isocyanate, methoxymethyl isocyanate, cyclohexyl isocyanate, phenyl isocyanate, tolyl isocyanate, nitrophenyl isocyanate, benzoyl isocyanate, phenylsulphonyl isocyanate, toluylene diisocyanate, pyrocarbonic acid methyl ester, pyrocarbonic acid ethyl ester, acetic anhydride, N,N'-diphenylurea, N,N'-dimethylurea, monomethylurea, or urea.
Claim 4
Dependent Claim
41 words
Process of claim 1 employing 0.01 to 5 mols of α-oximinoarylhydrazone, 0.01 to 0.5 mols of copper, or an ion of copper per mol of α-oximino-arylhydrazone, and at least 1 mol of said cyclizing agent, at a reaction temperature of 0°-150°C.
References Cited (Backward Citations)
US3666758A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1979-03-30 | 1979-09-29 | 1980-03-30 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-03-30 | 1983-09-29 | 1984-03-30 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-03-30 | 1987-09-29 | 1988-03-30 | $7700.00 | Window Closed / Lapsed |