GB875458A - Improvements in or relating to the preparation of 3-aminoisoxazoles - Google Patents

Improvements in or relating to the preparation of 3-aminoisoxazoles

Info

Publication number
GB875458A
GB875458A GB32111/59A GB3211159A GB875458A GB 875458 A GB875458 A GB 875458A GB 32111/59 A GB32111/59 A GB 32111/59A GB 3211159 A GB3211159 A GB 3211159A GB 875458 A GB875458 A GB 875458A
Authority
GB
United Kingdom
Prior art keywords
alkali
aminoisoxazoles
halogen
carboxylic acid
alkali metal
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
GB32111/59A
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.)
Shionogi and Co Ltd
Original Assignee
Shionogi and 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 Shionogi and Co Ltd filed Critical Shionogi and Co Ltd
Publication of GB875458A publication Critical patent/GB875458A/en
Expired legal-status Critical Current

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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

3-Aminoisoxazoles of the formula: <FORM:0875458/IV (b)/1> wherein R and R1, when individual, are each hydrogen or an alkyl, aryl or aralkyl radical and, when linked together, form a saturated or unsaturated hydrocarbon bridge (e.g. tetramethylene), are prepared by applying the Hofmann reaction to the corresponding isoxazole-3-carboxylic acid amides. Suitable reagents are halogen and alkali, halogen and alkali alcoholate or alkali metal (when alcohol solvents are used), alkali metal hypohalites and chloride of lime. Intermediates such as halogenoamides or urethane may occur as the main product and are transformed to the amine by heating with further amounts of alkali. N - Chloro - 5 - methylisoxazole-3-carboxylic acid amide may be isolated as an intermediate.
GB32111/59A 1958-09-20 1959-09-21 Improvements in or relating to the preparation of 3-aminoisoxazoles Expired GB875458A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP875458X 1958-09-20

Publications (1)

Publication Number Publication Date
GB875458A true GB875458A (en) 1961-08-23

Family

ID=13917945

Family Applications (1)

Application Number Title Priority Date Filing Date
GB32111/59A Expired GB875458A (en) 1958-09-20 1959-09-21 Improvements in or relating to the preparation of 3-aminoisoxazoles

Country Status (1)

Country Link
GB (1) GB875458A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3157669A (en) * 1962-07-17 1964-11-17 Hoffmann La Roche Preparation of isoxazole compounds
US3290326A (en) * 1963-09-20 1966-12-06 Hoffmann La Roche Esters of 4-lower alkyl-5-oxazole-car-bamic acid and intermediates therefor

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3157669A (en) * 1962-07-17 1964-11-17 Hoffmann La Roche Preparation of isoxazole compounds
US3290326A (en) * 1963-09-20 1966-12-06 Hoffmann La Roche Esters of 4-lower alkyl-5-oxazole-car-bamic acid and intermediates therefor

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