Methods for the preparation of charged crosslinkers
Processes for the preparation of charged crosslinkers bearing a sulfonic acid moiety are disclosed. These procedures also optionally include methods to convert the resulting products to substantially a single salt form.
1. A process for the preparation of a compound represented by formula (V):
or a salt thereof, comprising the steps of:
a) reacting a compound of the following formula:
with sodium hydroxide to form a compound of formula (1a):
or a salt thereof;
b) reacting the compound of formula (1a) or a salt thereof with 1,2-di(pyridin-2-yl)disulfane (PySSPy) to form a compound of formula (2a):
or a salt thereof,
c) reacting the compound of formula (2a) or a salt thereof, with chlorosulfonic acid to form a compound of formula (IV):
or a salt thereof; and
d) reacting the compound of formula (IV), or a salt thereof, with N-hydroxysuccinimide in the presence of the coupling agent 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) to form the compound of formula (V) or a salt thereof.
2. The process of claim 1 , wherein the sulfonating reaction of step c) is carried out in the presence of PySSPy.
3. The process of claim 2 , wherein about 0.5 equivalent of PySSPy is present.
4. The process of claim 1 , wherein in step d) the compound of formula (IV), or a salt thereof, is reacted with N-hydroxysuccinimide in the presence of a base to form a salt of the compound of formula (V) followed by purifying the salt of the compound of formula (V) by crystallization in the presence of an acid to form the neutral form of the compound of formula (V).
5. The process of claim 4 , wherein the base is diisopropylethylamine (DIPEA).
6. The process of claim 4 , wherein the acid is HCl.
7. The process of claim 5 , wherein the acid is HCl.
8. The process of claim 4 , wherein the crystallization is carried out in a mixture of an organic solvent and water.
9. The process of claim 6 , wherein the crystallization is carried out in a mixture of an organic solvent and water.
10. The process of claim 7 , wherein the crystallization is carried out in a mixture of an organic solvent and water.
11. The process of claim 1 , wherein 3.8 equivalents, 5.6 equivalents, 5.7 equivalents, or 6.0 equivalents of chlorosulfonic acid relative to the compound of formula (2a) is used in step c).
12. The process of claim 1 , wherein step c) of the method comprises: i) reacting the compound of formula (2a) with 3 equivalents of chlorosulfonic acid relative to the compound of formula (2a) at a temperature between 75° C. and 80° C., ii) adding an additional 1.33 equivalents of chlorosulfonic acid to the reaction mixture; and iii) adding a further 1.33 equivalents of chlorosulfonic acid.
13. The process of claim 1 , wherein the reaction between the compound of formula (2a) or a salt thereof, and chlorosulfonic acid in step c) is carried out between 70° C. and 90° C.
14. The process of claim 13 , wherein 3.8 equivalents, 5.6 equivalents, 5.7 equivalents, or 6.0 equivalents of chlorosulfonic acid relative to the compound of formula (2a) is used in step c).
15. The process of claim 13 , wherein step c) of the method comprises: i) reacting the compound of formula (2a) with 3 equivalents of chlorosulfonic acid relative to the compound of formula (2a) at a temperature between 75° C. and 80° C., ii) adding an additional 1.33 equivalents of chlorosulfonic acid to the reaction mixture; and iii) adding a further 1.33 equivalents of chlorosulfonic acid.
16. The process of claim 2 , wherein the reaction between the compound of formula (2a) or a salt thereof, and chlorosulfonic acid in step c) is carried out between 70° C. and 90° C.
17. The process of claim 3 , wherein the reaction between the compound of formula (2a) or a salt thereof, and chlorosulfonic acid in step c) is carried out between 70° C. and 90° C.