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ES408237A1 - 1,2-diphenyl-3,6-dioxo-4-hydroxy-5-n-butyl-tetrahydropyridazine - Google Patents

1,2-diphenyl-3,6-dioxo-4-hydroxy-5-n-butyl-tetrahydropyridazine

Info

Publication number
ES408237A1
ES408237A1 ES408237A ES408237A ES408237A1 ES 408237 A1 ES408237 A1 ES 408237A1 ES 408237 A ES408237 A ES 408237A ES 408237 A ES408237 A ES 408237A ES 408237 A1 ES408237 A1 ES 408237A1
Authority
ES
Spain
Prior art keywords
oxalic acid
tetrahydropyridazine
dioxo
diphenyl
hydroxy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
ES408237A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Takeda GmbH
Original Assignee
Byk Gulden Lomberg Chemische Fabrik GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Byk Gulden Lomberg Chemische Fabrik GmbH filed Critical Byk Gulden Lomberg Chemische Fabrik GmbH
Publication of ES408237A1 publication Critical patent/ES408237A1/en
Expired legal-status Critical Current

Links

Landscapes

  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Procedure for the preparation of 1,2-diphenyl-3,6-dioxo-4-hydroxy-5-n-butyl-tetrahydropyridazine, characterized in that caproic acid N, N'-diphenylhydrazide is reacted with an amount of two to four times greater than the molar oxalic acid dialkylhydric ester in the presence of an alkaline condensing agent in an inert organic solvent, because the alcohol formed during condensation is continuously distilled off as an azeotrope together with a part of the solvent, and because after the completion of the reaction, without previous distillation separation of the remaining solvent, the excess ester of oxalic acid is transformed into diamide of oxalic acid by ammonia. (Machine-translation by Google Translate, not legally binding)
ES408237A 1971-11-05 1972-11-03 1,2-diphenyl-3,6-dioxo-4-hydroxy-5-n-butyl-tetrahydropyridazine Expired ES408237A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19712155002 DE2155002A1 (en) 1971-11-05 1971-11-05 PROCESS FOR THE PREPARATION OF 1,2-DIPHENYL-3,6-DIOXO-4-HYDROXY-5-N-BUTYLTETRAHYDROPYRIDAZINE

Publications (1)

Publication Number Publication Date
ES408237A1 true ES408237A1 (en) 1975-11-16

Family

ID=5824281

Family Applications (1)

Application Number Title Priority Date Filing Date
ES408237A Expired ES408237A1 (en) 1971-11-05 1972-11-03 1,2-diphenyl-3,6-dioxo-4-hydroxy-5-n-butyl-tetrahydropyridazine

Country Status (10)

Country Link
JP (1) JPS4854091A (en)
AR (1) AR194854A1 (en)
AT (1) AT318635B (en)
BE (1) BE790923A (en)
DE (1) DE2155002A1 (en)
ES (1) ES408237A1 (en)
FR (1) FR2159994A5 (en)
GB (1) GB1354447A (en)
LU (1) LU66408A1 (en)
NL (1) NL7214865A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4180575A (en) 1977-03-22 1979-12-25 Hoechst Aktiengesellschaft Triazolidino-pyridazine-diones

Also Published As

Publication number Publication date
AR194854A1 (en) 1973-08-24
AT318635B (en) 1974-11-11
DE2155002A1 (en) 1973-05-17
JPS4854091A (en) 1973-07-30
LU66408A1 (en) 1973-11-12
BE790923A (en) 1973-05-03
GB1354447A (en) 1974-06-05
FR2159994A5 (en) 1973-06-22
NL7214865A (en) 1973-05-08

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