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US3017412A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the production of 3,5-diaminopyrazine-2.6-dicarboxylic acid derivatives

Assignee: Novartis AG
•
Filing: 1959-08-04
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Granted: 1962-01-16
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Expires: 1979-08-04
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Abstract

No abstract record available.

Inventors

  • 👤 Daglish Anthony Fenwick
  • 👤 Vonderwahl Rodolphe
  • 👤 Tillotson George Arnold

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 10:40
CPC Classifications
C; C07; C07D; C07D239/00; C07D239/02; C07D239/24; C07D239/28; C07D239/30; C07D241/00; C07D241/02; C07D241/10; C07D241/14; C07D241/24; C07D241/26; C07D401/00; C07D401/02; C07D401/12; C07D403/00; C07D403/02; C07D403/12; C07D405/00; C07D405/02; C07D405/12; C07D409/00; C07D409/02; C07D409/12; C07D475/00; C07D475/02; C07D487/00; C07D487/12; C07D487/14; C08; C08K; C08K5/00; C08K5/16; C08K5/34; C08K5/3467; C08K5/3477; C08K5/3492; C08K5/34926; C08L; C08L67/00; C08L67/02; C11; C11D; C11D3/00; C11D3/16; C11D3/26; C11D3/28; C11D3/40; C11D3/42; D; D06; D06L; D06L4/00; D06L4/60; D06L4/614; H; H01; H01M; H01M4/00; H01M4/86; H01M8/00; H01M8/14; Y; Y02; Y02E; Y02E60/00; Y02E60/30; Y02E60/50; Y02P; Y02P70/00; Y02P70/50

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 176 words
A PROCESS FOR THE PRODUCTION OF 3.5-DIAMINO-PYRAZINE-2,6-CICARBOXYLIC ACID AMIDES WHICH COMPRISES CONDENSING ONE MOLECULAR PROPORTION OF 1.3-DIALKYL-4-AMINO URACIL WITH SUBSTANTIALLY ONE MOLECULAR PROPORTION OF 1.3DIALKYL-4-AMINO-5-NITROSO URACIL IN AN ACIDIC MEDIUM WHILE SPLITTING OFF WATER AND AMMONIA TO FORM 3.2.;5.6-BIS((1''.3''RAMIDINO)-PYRAZINE AND SAPONIFYING THIS COMPOUND WITH AN ALKALI METAL HYDROXIDE TO FROM THE 3.5-DIAMINO-PYRAZINE-2.6-DICARBOXYLIC ACID AMIDE WHILE SPLITTING OFF TWO MOLECULAR PROPORTIONS OF CARBONIC ACID AND TRANSFORMING ANY CARBOXYLIC ACID GROUP FORMED DURING SAID ALKALINE TREATMENT INTO A CARBOXYLIC ACID AMIDE GROUP BY TREATING SAID SAPONIFICATION PRODUCT WITH A MEMBER SELECTED FROM THE GROUP CONSISTING OF THIONYL CHLORIDE, PHOSPHORUS TRICHLORIDE AND PHSOPHORUS TRIBROMIDE TO FORM THE CORRESPONDING CARBOXYLIC ACID HALIDE AND TREATING SAID CARBOXYLIC ACID HALIDE WITH A MEMBER SELECTED FROM THE GROUP CONSISTING OF AMMONIA, PRIMARY ALKYL AMINE, LOWER PRIMARY ALKENYLAMINE, LOWER PRIMARY HYDROXYALKYLAMINE, PRIMARY PHENYL-LOWER ALKYLAMINE, PRIMARY CYCLOHEXYLAMINE, PRIMARY PHENYLAMINE, PRIMARY ALKYLPHENYLAMINE, PRIMARY HALOPHENYLAMINE, PRIMARY ALKOXYPHENYLAMINE, PRIMARY PHENOXYPHENYLAMINE, PRIMARY CARBOXYPHENYLAMINE, PRIMARY SULPHOPHENYLAMINE, PRIMARY SULPHAMYLPHENYLAMINE, PRIMARY PYRAZOLYLAMINE, PRIMARY THIAZOLYLAMINE, PRIMARY THIADIAZOLYLAMINE, PRIMARY PYRIDYLAMINE, PRIMARY QUINOLYLAMINE, LOWER ALKYLUREA, BENZYLUREA AND PHENYLUREA TO FORM THE CORRESPONDING CARBOXYLIC ACID AMIDE.
Claim 2
Dependent Claim 176 words
A PROCESS FOR THE PRODUCTION OF 3.5-DIAMINO-PYRAZINE-2,6-CICARBOXYLIC ACID AMIDES WHICH COMPRISES CONDENSING ONE MOLECULAR PROPORTION OF 1.3-DIALKYL-4-AMINO URACIL WITH SUBSTANTIALLY ONE MOLECULAR PROPORTION OF 1.3DIALKYL-4-AMINO-5-NITROSO URACIL IN AN ACIDIC MEDIUM WHILE SPLITTING OFF WATER AND AMMONIA TO FORM 3.2.;5.6-BIS((1''.3''RAMIDINO)-PYRAZINE AND SAPONIFYING THIS COMPOUND WITH AN ALKALI METAL HYDROXIDE TO FROM THE 3.5-DIAMINO-PYRAZINE-2.6-DICARBOXYLIC ACID AMIDE WHILE SPLITTING OFF TWO MOLECULAR PROPORTIONS OF CARBONIC ACID AND TRANSFORMING ANY CARBOXYLIC ACID GROUP FORMED DURING SAID ALKALINE TREATMENT INTO A CARBOXYLIC ACID AMIDE GROUP BY TREATING SAID SAPONIFICATION PRODUCT WITH A MEMBER SELECTED FROM THE GROUP CONSISTING OF THIONYL CHLORIDE, PHOSPHORUS TRICHLORIDE AND PHSOPHORUS TRIBROMIDE TO FORM THE CORRESPONDING CARBOXYLIC ACID HALIDE AND TREATING SAID CARBOXYLIC ACID HALIDE WITH A MEMBER SELECTED FROM THE GROUP CONSISTING OF AMMONIA, PRIMARY ALKYL AMINE, LOWER PRIMARY ALKENYLAMINE, LOWER PRIMARY HYDROXYALKYLAMINE, PRIMARY PHENYL-LOWER ALKYLAMINE, PRIMARY CYCLOHEXYLAMINE, PRIMARY PHENYLAMINE, PRIMARY ALKYLPHENYLAMINE, PRIMARY HALOPHENYLAMINE, PRIMARY ALKOXYPHENYLAMINE, PRIMARY PHENOXYPHENYLAMINE, PRIMARY CARBOXYPHENYLAMINE, PRIMARY SULPHOPHENYLAMINE, PRIMARY SULPHAMYLPHENYLAMINE, PRIMARY PYRAZOLYLAMINE, PRIMARY THIAZOLYLAMINE, PRIMARY THIADIAZOLYLAMINE, PRIMARY PYRIDYLAMINE, PRIMARY QUINOLYLAMINE, LOWER ALKYLUREA, BENZYLUREA AND PHENYLUREA TO FORM THE CORRESPONDING CARBOXYLIC ACID AMIDE.

References Cited (Backward Citations)

US2581889A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1965-01-15 1965-07-17 1966-01-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1969-01-15 1969-07-17 1970-01-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1973-01-15 1973-07-17 1974-01-16 $7700.00 Window Closed / Lapsed

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