Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives
424180, C07H 1522
O-2,6-diamino-2,3,6-trideoxy-.alpha.-D-ribo-hexo-pyranosyl-(1.fwdarw.4)-O-[ 5-amino-5-deoxy-.beta.-D-xylofuranosyl-(1.fwdarw.5)]-N.sup.1 -[(S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxystreptamine), also named 5"-amino-3',5"-dideoxybutirosin A and acid addition salts of said compounds. These compounds exhibit a wide spectrum of antibacterial activity.
The above compounds can be produced from O-2,6-dideoxy-2,6-bis(Z-amino)-.alpha.-D-glucopyranosyl-(1.fwdarw.4)-O-[2, 3-di-O-acetyl-5-deoxy-5-(Z-amino)-.beta.-D-xylofuranosyl-(1.fwdarw. 5)]-6-O-acetyl-N.sup.1 -[(S)-2-acetyloxy-1-oxo-4-(Z-amino)butyl]-2-deoxy-N.sup. 3 -streptamine, also named protected 5"-amino-deoxybutirosin A by treating said compound with trifluoromethanesulfonic anhydride and pyridine to yield the 3'-O-(trifluoromethanesulfonyl) compound. The product is reacted with the sodium salt of an arylmercaptan and the resulting 3'-arylthio compound is purified and treated with ammonia, thus deprotecting the four hydroxy groups. Lastly, the five amino groups are deprotected and the arylthio group is removed by a reductive cleavage.
patent: 3828021 (1974-08-01), Beattie et al.
B371,085, Jan. 1975, Naito et al. 260/210 AB.
Ikeda et al., "Jour. Antibiotics," vol. XXVI, No. 5, 1973, pp. 307-309.
Haskell Theodore Herbert
Kee Woo Peter Wing
Brown Johnnie R.
Parke, Davis & Company
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