Carbohydrate conjugated RNA agents and process for their preparation
View Patent ↗This disclosure relates to an improved process for the preparation of carbohydrate conjugates. The disclosure also relates to carbohydrate conjugated iRNA agents comprising these carbohydrate conjugates, which have improved purity and are advantageous for the in vivo delivery of the iRNA agents.
1. A process for preparing a compound of formula (A):
wherein
each occurrence of X is hydrogen or a hydroxy protecting group;
each occurrence of Y is an amine protecting group;
n is 0-20;
each occurrence of q, r and s is independently 1-7;
L is a linking group; and
R 1 is an iRNA agent;
the process comprising
(a) converting a compound of formula (VI) to a compound of formula (VII):
by a process comprising:
(i) reacting the compound of formula (VI) with a base;
(ii) reducing the product of step (i); and
(iii) reacting the product of step (ii) with an acid; and
(b) converting the compound of formula (VII) to a compound of formula (A);
wherein the compound of formula (A) is free or substantially free of one or more of
(i) metal impurities,
(ii) each of the following two urea side products
and
(iii) each of the following saccharide compounds
2. The process of claim 1 , wherein the base is a metal alkoxide.
3. The process of claim 1 , wherein the base is sodium methoxide, step (ii) involves reacting the product of step (i) with sodium borohydride, and the acid is hydrochloric acid.
4. A process for preparing a compound of formula (A):
wherein
each occurrence of X is hydrogen or a hydroxy protecting group;
each occurrence of Y is an amine protecting group;
n is 0-20;
each occurrence of q, r and s is independently 1-7;
L is a linking group; and
R 1 is an iRNA agent;
the process comprising
(a) reacting a compound of the formula (IX):
with a compound of the formula (X):
wherein Hal is halogen to yield a compound of formula (VIII)
wherein
A is a C 6 -C 14 alkylene linker;
each R is, independently, an acid protecting group; and
R x is an acid protecting group; and
(b) converting the compound of formula (VIII) to a compound of formula (A);
wherein the compound of formula (A) is free or substantially free of one or more of
(i) metal impurities,
(ii) each of the following two urea side products
and
(iii) each of the following saccharide compounds
5. The process of claim 4 , wherein R is t-butyl, Hal is Cl and A is a C 10 alkylene linker.
6. The process of claim 4 , wherein the reaction is conducted in the presence of N,N-diisopropylethylamine.
7. A process for preparing a compound of formula (A):
wherein
each occurrence of X is hydrogen or a hydroxy protecting group;
each occurrence of Y is an amine protecting group;
n is 0-20;
each occurrence of q, r and s is independently 1-7;
L is a linking group; and
R 1 is an iRNA agent;
the process comprising:
a) reacting a compound of the formula (XII):
wherein P is an amino protecting group with a sulfonic acid to give a compound of formula (II):
wherein
Z is an acid protecting group,
n is 0-20, and
each occurrence of q, r and s is independently 1-7; and
b) converting the compound of formula (II) to a compound of formula (A);
wherein the compound of formula (A) is free or substantially free of one or more of
(i) metal impurities,
(ii) each of the following two urea side products
and
(iii) each of the following saccharide compounds
8. The process of claim 7 , wherein the sulfonic acid is p-toluene sulfonic acid or methanesulfonic acid.
9. A process for preparing a compound of formula (A):
wherein
each occurrence of X is hydrogen or a hydroxy protecting group;
each occurrence of Y is an amine protecting group;
n is 0-20;
each occurrence of q, r and s is independently 1-7;
L is a linking group; and
R 1 is an iRNA agent;
the process comprising:
a) reacting a compound of formula (XIV)
with dihydrofuran-2,5-dione in the presence of a tertiary amine to give a compound of formula (XIII):
wherein
X is a hydroxyl protecting group;
Y is an amine protecting group;
Prt is a hydroxyl protecting group;
n is 0-15; and
q, r and s are each, independently, 1-7; and
b) converting the compound of formula (XIII) to a compound of formula (A);
wherein the compound of formula (A) is free or substantially free of one or more of
(i) metal impurities,
(ii) each of the following two urea side products
and
(iii) each of the following saccharide compounds
10. The process of claim 9 , wherein the tertiary amine is triethylamine or pyridine.