GB350782A - A process for the production of di-substituted tetrazoles - Google Patents

A process for the production of di-substituted tetrazoles

Info

Publication number
GB350782A
GB350782A GB21835/30A GB2183530A GB350782A GB 350782 A GB350782 A GB 350782A GB 21835/30 A GB21835/30 A GB 21835/30A GB 2183530 A GB2183530 A GB 2183530A GB 350782 A GB350782 A GB 350782A
Authority
GB
United Kingdom
Prior art keywords
pentamethylenetetrazole
lactam
production
imide
halogen
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
GB21835/30A
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.)
Abbott GmbH and Co KG
Original Assignee
Knoll 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 Knoll GmbH filed Critical Knoll GmbH
Publication of GB350782A publication Critical patent/GB350782A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Disubstituted tetrazoles of the pentamethylenetetrazole type are prepared by treating the corresponding halogen-substituted imide-chlorides with hydrazoic acid or azides, and then eliminating the halogen by reduction. According to the example, e -leucine lactam is heated with phosphorus pentachloride in xylene, the imide-chloride of dichlorleucine lactam isolated and added to a solution of hydrazoic acid in benzene; the resulting dichlorpentamethylenetetrazole is then reduced with zinc dust and acetic acid giving pentamethylenetetrazole. Specifications 250,897, 257,418, and 287,924, [all in Class 2 (iii), Dyes &c.], are referred to.
GB21835/30A 1930-05-20 1930-07-18 A process for the production of di-substituted tetrazoles Expired GB350782A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE350782X 1930-05-20

Publications (1)

Publication Number Publication Date
GB350782A true GB350782A (en) 1931-06-18

Family

ID=6264290

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21835/30A Expired GB350782A (en) 1930-05-20 1930-07-18 A process for the production of di-substituted tetrazoles

Country Status (1)

Country Link
GB (1) GB350782A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3966756A (en) * 1975-04-07 1976-06-29 American Cyanamid Company Substituted dibenzo[b,f]tetrazolo[1,5-d][1,4]-oxazepines

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3966756A (en) * 1975-04-07 1976-06-29 American Cyanamid Company Substituted dibenzo[b,f]tetrazolo[1,5-d][1,4]-oxazepines

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