Compositions of trofinetide
This disclosure describes compounds of Formula (I), stereoisomers, side compounds thereof, pharmaceutical compositions and methods of manufacturing such compounds, using silylation reagents and producing compositions and products made using such methods. More particularly, this disclosure describes manufacture of trofinetide and side products, compositions and products containing such compounds, for pharmaceutical uses to treat neurodegenerative or neurodevelopmental disorders.
1. A composition comprising a compound of Formula (I):
or a stereoisomer, or pharmaceutically acceptable salt thereof, and between about 0.001 wt % and about 2 wt % of a compound of Formula (II):
or a stereoisomer, or pharmaceutically acceptable salt thereof, and between about 0.001 wt % and about 2 wt % of a compound of Formula (III):
or a stereoisomer, or pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 and R 4 independently are selected from the group consisting of hydrogen and C 1-4 alkyl, provided at least one of R 1 , R 2 , R 3 and R 4 is C 1-4 alkyl.
2. The composition according to claim 1 , wherein the compound of Formula (I) is a compound of Formula (Ia):
or pharmaceutically acceptable salt thereof.
3. The composition according to claim 1 , wherein the compound of Formula (II) is a compound of Formula (IIa):
or pharmaceutically acceptable salt thereof.
4. The composition according to claim 1 , wherein the compound of Formula (III) is a compound of Formula (IX):
or pharmaceutically acceptable salt thereof.
5. The composition according to claim 1 , comprising the compound of Formula (III), wherein the compound according to Formula (III) is a compound of Formula (IIIa):
or pharmaceutically acceptable salt thereof.
6. The composition according to claim 2 comprising between about 97 wt % and about 100 wt % of the compound of Formula (Ia) on an anhydrous basis.
7. The composition according to claim 1 , wherein the compound according to Formula (III) is a compound of Formula (IV):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (V):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (VI):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (VII):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (VIII):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (IX):
or a stereoisomer, or pharmaceutically acceptable salt thereof.
8. The composition according to claim 2 , wherein said composition is obtained by:
a) coupling (2S)-2-methylpyrrolidine-2-carboxylic acid and benzyloxycarbonyl-glycine in the presence of an activating reagent, silylating agent and a solvent, or
b) coupling benzyloxycarbonyl-glycine and N-hydroxysuccinimide and then coupling the obtained benzyloxycarbonyl-glycine N-succinimidyl ester and (2S)-2-methylpyrrolidine-2-carboxylic acid in the absence or presence of an activating reagent, a solvent and in the absence or presence of a silylating agent;
c) coupling the obtained ((S)-1-(((benzyloxy)carbonyl)glycyl)-2-methylpyrrolidine-2-carboxylic acid) and (2S)-2-aminopentanedioic acid in the presence of an activating reagent, silylating agent and a solvent;
d) obtaining ((S)-1-(((benzyloxy)carbonyl)glycyl)-2-methylpyrrolidine-2-carbonyl)-L-glutamic acid; and
e) deprotecting ((S)-1-(((benzyloxy)carbonyl)glycyl)-2-methylpyrrolidine-2-carbonyl)-L-glutamic acid, to obtain a composition comprising the compound of Formula (Ia).
9. The composition according to claim 8 , wherein the compound according to Formula (II) is a compound of Formula (IIa):
or pharmaceutically acceptable salt thereof.
10. The composition according to claim 8 , wherein deprotecting is achieved by hydrogenation.
11. The composition according to claim 10 , wherein hydrogenation is performed in the presence of a Pd/C catalyst.
12. The composition according to claim 10 , wherein hydrogenation is performed in the presence of a Pd/Si catalyst.
13. The composition according to claim 10 , wherein the hydrogenation is performed using at least one solvent selected from the group consisting of water, ethyl acetate, isopropyl acetate, methanol, ethanol, isopropanol, or mixtures thereof.
14. A kit containing a dosage form comprising a compound of Formula (Ia):
or a pharmaceutically acceptable salt thereof, and between about 0.001 wt % and about 2 wt % of a compound of Formula (IIa):
or pharmaceutically acceptable salt thereof, and instructions for administration to a subject in need thereof.
15. The composition according to claim 1 , wherein the compound of Formula (II), or stereoisomer, or pharmaceutically acceptable salt thereof, is present in an amount between about 0.001 wt % and about 0.2 wt %; and the compound of Formula (III), or stereoisomer, or pharmaceutically acceptable salt thereof, is absent.
16. A composition according to claim 1 , comprising a compound of Formula (Ia):
or pharmaceutically acceptable salt thereof, between about 0.001 wt % and about 0.2 wt % of a compound of Formula (IIa):
or pharmaceutically acceptable salt thereof; and
between about 0.001 wt % and about 0.2 wt % of a compound of Formula (IIIa):
or pharmaceutically acceptable salt thereof.
17. A composition comprising a compound of Formula (I):
or a stereoisomer, or pharmaceutically acceptable salt thereof, and between about 0.001 wt % and about 2 wt % of a compound of Formula (III):
or a stereoisomer, or pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 and R 4 independently are selected from the group consisting of hydrogen and C 1-4 alkyl, provided at least one of R 1 , R 2 , R 3 and R 4 is C 1-4 alkyl.
18. The composition according to claim 17 , wherein the compound of Formula (I) is a compound of Formula (Ia):
or pharmaceutically acceptable salt thereof.
19. The composition according to claim 17 , wherein the compound according to Formula (III) is a compound of Formula (IV):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (V):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (VI):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (VII):
or a stereoisomer, or pharmaceutically acceptable salt thereof;
Formula (VIII):
or a stereoisomer, or pharmaceutically acceptable salt thereof; or
Formula (IX):
or a stereoisomer, or pharmaceutically acceptable salt thereof.
20. The composition according to claim 17 , wherein the compound of Formula (III), or stereoisomer, or pharmaceutically acceptable salt thereof, is present in an amount between about 0.001 wt % and about 0.2 wt %.