Polyamine compounds and methods for their production

Details Polyamine compounds and methods for their production Polyamine compounds and methods for their production

C - Chemistry, Metallurgy

07

H

260/230.56

C07H 15/22 (2006.01) C07H 15/23 (2006.01)

Patent

CA 1049005

"NEW POLYAMINE COMPOUNDS AND METHODS FOR THEIR PRODUCTION" Abstract of the Disclosure 0-2,6-Diamino-2,3,4,6-tetradeoxy-.alpha.-D-erythro- hexopyranosyl-(1?4)-0-[5-amino-5-deoxy-.beta.-D-xylofuranosyl- (1?5)]-N1-[(S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy- streptamine, also known as aminotrideoxybutirosin A, and acid-addition salts. They have a wide spectrum of anti- bacterial activity. The above compounds can be produced from amino- deoxybutirosin A by the sequence of reactions which comprises protecting the five primary amino groups by converting them to arylmethoxycarbonyl derivatives, converting the 3',4'- hydroxyl groups to an acetal, acylating the remaining four hydroxyl groups,and hydrolyzing the acetal to produce a key intermediate which is an 0-2,6-dideoxy-2,6-bis[[(arylmethoxy)- carbonyl]amino]-.alpha.-D-glucopyranosyl-(1?4)-0-[2,3-di-0-acyl-5- deoxy-5-[[(arylmethoxy)carbonyl]amino]-.beta.-D-xylofuranosyl-(1?5)]- 6-0-acyl-N1-[(S)-2-acyloxy-1-oxo-4-[[(arylmethoxy)carbonyl] amino]-butyl]-2-deoxy-N3-[(arylmethoxy)carbonyl]streptamine, generically also identified as protected 5"-aminodeoxy- butirosin A. That compound is reacted with methanesulfonyl chloride in pyridine to introduce 3',4'-methanesulfonyloxy groups which are removed by reaction with zinc and sodium iodide to introduce a double bond at the 3',4' position. The acyl groups are hydrolyzed or cleaved as by reaction with ammonia in methanol and the product is reacted with hydrogen in the presence of a catalyst to remove the arylmethoxy- carbonyl groups and hydrogenate the double bond with the formation of aminotrideoxybutirosin A. -1a-

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