IP Library Granted Patent US 10,815,262
Granted Patent B2
US 10,815,262 · App. 15/905,922 · Granted Oct 27, 2020

Methods of preparing nicotinamide riboside and derivatives thereof

Inventors: Marie Migaud (Lurgan, GB); Philip Redpath (Portadown, GB); Kerri Crossey (Magherafelt, GB); Mark Doherty (Newtownabbey, GB)
Assignee: THE QUEEN'S UNIVERSITY OF BELFAST
C07H19/048C07H1/00C07H1/06C07H19/04Y02P20/582
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,815,262
App. No.
15/905,922
Granted
Oct 27, 2020
Kind
B2
Abstract

The invention relates to methods of preparing nicotinamide riboside and derivatives thereof. In an aspect, the invention relates to a method of preparing a compound of formula (I), wherein n is 0 or 1; m is 0 or 1; Y is O or S; R 1 is selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted primary or secondary amino, and substituted or unsubstituted azido; R 2 -R 5 , which may be the same or different, are each independently selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, and substituted or unsubstituted aryl; and X − is an anion, selected from an anion of a substituted or unsubstituted carboxylic acid, a halide, a substituted or unsubstituted sulfonate, a substituted or unsubstituted phosphate, a substituted or unsubstituted sulfate, a substituted or unsubstituted carbonate, and a substituted or unsubstituted carbamate.

Claims (39)

1. A compound of formula (III)

wherein:

n is 0 or 1;

m is 0 or 1;

Y is O or S;

R 1 is selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted primary or secondary amino, and substituted or unsubstituted azido;

R 2 -R 5 , which may be the same or different, are each independently selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, and substituted or unsubstituted aryl; and

R 6 , R 7 and R 8 , which may be the same or different, are each independently a hydroxyl protecting group or are each H, provided that when n is 1, m is 1, Y is O, R 1 is methyl, and R 2 -R 5 are each H, then R 6 , R 7 , and R 8 are not all simultaneously H or unsubstituted acetyl; further provided that when n is 1, m is 1, Y is O, R 1 is methyl, R 3 and R 4 are methyl, and R 2 and R 5 are each H, then R 6 , R 7 and R 8 are not all simultaneously H or unsubstituted acetyl; and yet further provided that when n is 0, m is 1, R 1 is NH 2 , and R 2 -R 5 are each H, then R 6 , R 7 , and R 8 are not all simultaneously H or unsubstituted benzoyl.

2. A compound of claim 1 , wherein R 6 , R 7 and R 8 are each H.

3. A compound according to claim 1 , wherein R 6 , R 7 and R 8 are each independently an ester-type protecting group, an ether-type protecting group, or a silyl-type protecting group.

4. A compound according to claim 3 , wherein the R 6 , R 7 and R 8 moieties are selected from substituted and unsubstituted acetyl, and substituted and unsubstituted benzoyl.

5. A compound according to claim 3 , wherein the ester-type protecting group is a protecting group selected from acetyl, propionyl, isopropionyl, benzoyl, and trihaloacetyl.

6. A compound according to claim 5 , wherein the R 6 , R 7 and R 8 moieties are selected from substituted and unsubstituted acetyl, and substituted and unsubstituted benzoyl.

7. A compound according to claim 3 , wherein the ester-type protecting group is a protecting group selected from trifluoroacetyl or trichloroacetyl, and provided that when n is 0 and m is 1, R 1 is not NH 2 .

8. A compound according to claim 3 , wherein the ether-type protecting group is a protecting group selected from benzyl, p-methoxybenzyl, methoxymethyl and allyl ethers.

9. A compound according to claim 3 , wherein the silyl-type protecting group is a protecting group selected from trimethylsilyl, triethylsilyl, triisopropylsilyl, 2-(trimethylsilyl)ethoxymethyl, tert-butyldimethylsilyl, tert-butyldiphenylsilyl and tetraisopropyldisilyl.

10. A compound of claim 1 , wherein at least two of R 6 , R 7 and R 8 are selected from unsubstituted acetyl or unsubstituted benzoyl.

11. A compound according to claim 1 , which is triacetyl O-ethyl-1,4-dihydronicotinate riboside:

12. A compound of formula (IV)

wherein

n is 1;

m is 1;

Y is O;

R 1 is selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted primary or secondary amino, and substituted or unsubstituted azido;

R 2 -R 5 are each H; and

R 6 , R 7 and R 8 , which may be the same or different, are each independently a hydroxyl protecting group; and

X − is an anion selected from an anion of a substituted or unsubstituted carboxylic acid, a halide, a substituted or unsubstituted sulfonate, a substituted or unsubstituted phosphate, a substituted or unsubstituted sulfate, a substituted or unsubstituted carbonate, and a substituted or unsubstituted carbamate;

provided that when n is 1, m is 1, Y is O, R 1 is H or NH 2 , R 2 -R 5 are each H, and X − is a substituted sulfonate, then R 6 , R 7 , and R 8 are not all simultaneously H or unsubstituted acetyl or unsubstituted benzoyl.

13. A compound of formula:

wherein X − is an anion selected from an anion of a substituted or unsubstituted carboxylic acid, a halide, a substituted or unsubstituted sulfonate, a substituted or unsubstituted phosphate, a substituted or unsubstituted sulfate, a substituted or unsubstituted carbonate, and a substituted or unsubstituted carbamate, provided that X − is not trifluoromethylsulfonate.

14. A compound of claim 1 , wherein:

Y n R 1 is NH 2 or —OCH 2 CH 3 ; and

R 2 -R 5 are all hydrogens.

15. The compound of claim 14 , wherein R 6 , R 7 and R 8 , are each the same group.

16. A compound of claim 10 , wherein at least two of R 6 , R 7 and R 8 are selected from unsubstituted acetyl or unsubstituted benzoyl and provided that when n is 0 and m is 1, R 1 is not NH 2 .

17. The compound of claim 12 , wherein X − is an anion selected from an anion of a substituted or unsubstituted carboxylic acid, a substituted or unsubstituted phosphate, a substituted or unsubstituted sulfate, a substituted or unsubstituted carbonate, and a substituted or unsubstituted carbamate.

18. The compound of claim 12 , wherein X − is an anion selected from acetate, formate, trifluoroacetate, glutamate, lactate, and aspartate.

19. The compound of claim 13 , wherein X − is an anion selected from an anion of a substituted or unsubstituted carboxylic acid, a halide, a substituted or unsubstituted phosphate, a substituted or unsubstituted sulfate, a substituted or unsubstituted carbonate, and a substituted or unsubstituted carbamate.

20. The compound of claim 13 , wherein X − is an anion selected from acetate, formate, trifluoroacetate, glutamate, lactate and aspartate.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2026
From: QUEEN'S UNIVERSITY BELFAST
To: CHROMADEX INC.
Reel/Frame 075102/0433 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2018
From: MIGAUD, MARIE; REDPATH, PHILIP; CROSSEY, KERRI; DOHERTY, MARK
To: THE QUEEN'S UNIVERSITY OF BELFAST
Reel/Frame 045047/0562 →