GB787282A - Process for the manufacture of isonicotinyl hydrazide - Google Patents

Process for the manufacture of isonicotinyl hydrazide

Info

Publication number
GB787282A
GB787282A GB1875155A GB1875155A GB787282A GB 787282 A GB787282 A GB 787282A GB 1875155 A GB1875155 A GB 1875155A GB 1875155 A GB1875155 A GB 1875155A GB 787282 A GB787282 A GB 787282A
Authority
GB
United Kingdom
Prior art keywords
cyanopyridine
catalyst
water
manufacture
hydrazine
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
GB1875155A
Inventor
Edward James Gasson
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB1875155A priority Critical patent/GB787282A/en
Publication of GB787282A publication Critical patent/GB787282A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/86Hydrazides; Thio or imino analogues thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Catalysts (AREA)
  • Pyridine Compounds (AREA)

Abstract

Isonicotinyl hydrazide is made by reacting hydrazine with 4-cyanopyridine at an elevated temperature, preferably between 80 DEG C. and the boiling-point of the solution, in the presence of water, with or without a water-miscible organic solvent and optionally in the presence of an alkaline compound, such as an oxide, hydroxide or carbonate of an alkali or alkaline earth metal or magnesium, as a catalyst. The concentration of the 4-cyanopyridine in the reaction mixture is preferably kept below 10 per cent. Examples describe the reaction of 4-cyanopyridine with hydrazine in the absence of a catalyst and in the presence of magnesium oxide, and sodium hydroxide as catalysts. Specifications 776,313 and 785,346 are referred to.
GB1875155A 1955-06-29 1955-06-29 Process for the manufacture of isonicotinyl hydrazide Expired GB787282A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1875155A GB787282A (en) 1955-06-29 1955-06-29 Process for the manufacture of isonicotinyl hydrazide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1875155A GB787282A (en) 1955-06-29 1955-06-29 Process for the manufacture of isonicotinyl hydrazide

Publications (1)

Publication Number Publication Date
GB787282A true GB787282A (en) 1957-12-04

Family

ID=10117775

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1875155A Expired GB787282A (en) 1955-06-29 1955-06-29 Process for the manufacture of isonicotinyl hydrazide

Country Status (1)

Country Link
GB (1) GB787282A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021069975A1 (en) * 2019-10-10 2021-04-15 Nelson Mandela University A continuous flow synthesis method for the manufacture of isoniazid

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021069975A1 (en) * 2019-10-10 2021-04-15 Nelson Mandela University A continuous flow synthesis method for the manufacture of isoniazid
CN114981244A (en) * 2019-10-10 2022-08-30 纳尔逊·曼德拉大学 Continuous flow synthesis method for preparing isoniazid

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