SYNTHESIS OF ANTIBACTERIAL AMINOGLYCOSIDE ANALOGS
The present disclosure relates to novel methods for preparing antibacterial aminoglycoside compounds, as well as to related intermediates, and crystal forms thereof, useful in such methods.
1 - 108 . (canceled)
109 . A process for preparing a compound (6), or a salt thereof, or solvate thereof, or an enantiomer thereof, or a diastereomer thereof comprising:
(d) contacting a compound of formula (4),
or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof, with Boc protecting group reagent to yield a compound of formula (5):
or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof;
(e) contacting the compound of formula (5), or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof, with a PNZ deprotecting reagent to yield a compound of formula (6):
or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
110 . The process of claim 109 , wherein the PNZ deprotecting reagent is sodium dithionite.
111 . The process of claim 109 , further comprising preparing a crystalline form of compound of formula (6), or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
112 . The process of claim 109 , further comprising isolating the compound of formula (6), or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
113 . The process of claim 109 , further comprising:
(f) contacting the compound of formula (6), or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof, with
wherein LG 1 is a leaving group, to yield a compound of formula (7):
or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
114 . The process of claim 113 , wherein the leaving group is iodo.
115 . The process of claim 113 , wherein the
is present in about 1.0 to 1.5 molar equivalents to the compound of formula (6).
116 . The process of claim 113 , wherein step (f) is performed in conditions substantially free of water.
117 . The process of claim 113 , wherein step (f) is performed in the presence of a solvent selected from the group consisting of acetonitrile, acetone, and combination thereof.
118 . The process of claim 113 , wherein step (f) is performed in the presence of NaHCO 3 .
119 . The process of claim 113 , wherein step (f) is performed at a temperature of about 30° C. to 40° C.
120 . The process of claim 113 , further comprising adding 1,4-diazabicyclo[2.2.2]octane (DABCO) to a reaction mixture.
121 . The process of claim 113 , further comprising preparing a crystalline form of compound of formula (7), or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
122 . The process of claim 113 , further comprising isolating the compound of formula (7), or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
123 . The process of claim 113 , further comprising:
(g) contacting the compound of formula (7), or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof, with a Boc removing reagent to yield a compound of formula (8):
or a salt thereof, or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
124 . The process of claim 123 , wherein the Boc removing reagent is TFA, thereby yielding a TFA salt of compound of formula (8), or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
125 . The process of claim 124 , further comprising removing the TFA salt to afford a compound of formula (8), or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
126 . The process of claim 123 , further comprising:
(h) performing a salt formation with an acid to yield a salt of a compound of formula (8), or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof.
127 . The process of claim 126 , wherein the acid in step (h) is sulfuric acid, thereby yielding a sulfate salt of a compound of formula (9):
or a solvate thereof, or an enantiomer thereof, or a diastereomer thereof, wherein x is 1 to 5.
128 . The process of claim 109 , wherein is a double bond.
129 . The process of claim 109 , wherein the stereochemistry at carbon atoms 1, 3, 4, 5, 6, 1′, 2′, 1″, 2″, 3″, 4″, and 1-z in formulae (4)-(9) are indicated as in formula (Y), wherein indicates a point of attachment to hydrogen or a moiety:
130 . Crystalline tert-butyl ((2R,3R,4R,5R)-2-(((1S,2S,3R,4S,6R)-3-(((2S,3R)-6-(aminomethyl)-3-((tert-butoxycarbonyl)amino)-3,4-dihydro-2H-pyran-2-yl)oxy)-4-((tert-butoxycarbonyl)amino)-6-((S)-4-((tert-butoxycarbonyl)amino)-2-hydroxybutanamido)-2-hydroxycyclohexyl)oxy)-3,5-dihydroxy-5-methyltetrahydro-2H-pyran-4-yl)(methyl)carbamate, Formula (6a), or a solvate thereof.