Chiral fluorinating reagents

Patent metadata

Field	Value
Publication number	US-9701684-B2
Application number	US-201314440530-A
Country	US
Kind code	B2
Filing date	Nov 5, 2013
Priority date	Nov 5, 2012
Publication date	Jul 11, 2017
Grant date	Jul 11, 2017

Abstract

This invention relates to fluorinating agents and, more particularly, to chiral non-racemic fluorinating agents useful for enantioselective fluorination, as well as to their synthesis and use and other subject matter. The fluorinating agents are based on a substituted 1,4-diazabicyclo[2.2.2]octane (DABCO) skeleton and provide electrophillic fluorine enantioselectively.

First claim

The invention claimed is:

1. A product comprising a non-racemic chiral species, wherein the chiral species has the structure:

wherein each of R 6a , R 6b , R 6c , R 6d , R 7a , R 7b , R 7c , R 7d , R 8a , R 8b , R 8c and R 8d is independently selected from the group consisting of: H, aryl and —(CH 2 ) n -aryl, wherein n is from 1 to 4, and wherein aryl is optionally substituted by at least one substituent selected from fluorine, alkyl and alkyl substituted by at least one fluorine; and
R 4 is an independently selected substituent other than fluorine;
provided that for at least one pair selected from: R 6a and R 6b ; R 6c and R 6d ; R 7a and R 7b ; R 7c and R 7d ; R 8a and R 8b ; and R 8c and R 8d , one member of that pair is different from the other member of that pair.

2. A product comprising a non-racemic chiral species, wherein the chiral species has the structure:

wherein each of R 6a , R 6b , R 6c , R 6d , R 7a , R 7b , R 7c , R 7d , R 8a , R 8b , R 8c and R 8d is independently selected from the group consisting of: H and the following moieties:

wherein:
which t is 0, 1, 2, 3, 4 or 5,
u is 0, 1, 2 or 3,
v is0, 1, 2, 3 or 4, and
R 9 and R 10 are independently selected from halo, cyano, carboxy, sulphoxy, nitro, alkyl and alkyl substituted one or more times by halo; and
R 4 is an independently selected substituent other than fluorine;
provided that for at least one pair selected from: R 6a and R 6b ; R 6c and R 6d ; R 7a and R 7b ; R 7c and R 7d ; R 8a and R 8b ; and R 8c and R 8d , one member of that pair is different from the other member of that pair.

3. The product of claim 2 wherein the chiral species has the structure:

wherein both members of the pair R 6a and R 6d are the same and both members of the pair R 6b and R 6c are the same as each other but different from R 6a and R 6d .

4. The product of claim 2 wherein the chiral species has the structure:

wherein both members of the pair R 7a and R 7d are the same and both members of the pair R 7b and R 7c are the same as each other but different from R 7a and R 7d .

5. The product of claim 2 wherein the chiral species has the structure:

wherein both members of the pair R 6a and R 7c are the same and both members of the pair R 6b and R 7d are the same as each other but different from R 6a and R 7c .

6. The product of claim 2 wherein the chiral species has the structure:

wherein both members of the pair R 6c and R 7a are the same and both members of the pair R 6d and R 7b are the same as each other but different from R 6c and R 7a .

7. A product comprising a non-racemic chiral species, wherein the chiral species has the structure:

wherein each of R 6a , R 6b , R 6c , R 6d , R 7a , R 7b , R 7c , R 7d , R 8a , R 8b , R 8c and R 8d is an independently selected substituent; and
R 4 is an independently selected substituent other than fluorine;
provided that for at least one pair selected from: R 6a and R 6b ; R 6c and R 6d ; R 7a and R 7b ; R 7c and R 7d ; R 8a and R 8b ; and R 8c and R 8d , one member of that pair is different from the other member of that pair;
wherein at least one member of R 6a ,R 6b , R 6c , R 6d , R 7a , R 7b , R 7c , R 7d , R 8a ,R 8b , R 8c and R 8d is a proximally asymmetric substituent, and
wherein the or each proximally asymmetric substituent, selected independently of any other proximally asymmetric substituent, has the formula (XVIII):

wherein R 11 , R 12 and R 13 are each different and are selected from: H and M-R 14 ,
M is a bond or an inert linker containing 1, 2, 3, 4 or 5 in-chain atoms; and
R 14 is H or a moiety having from 1 to 20 plural valent atoms, selected from heteroaryl, heteroaryl substituted with one or more substituents, hydrocarbyl, hydrocarbyl substituted with one or more substituents selected from alkoxy, halogen, cyano, carboxy, sulphoxy and nitro.

8. The product of claim 2 wherein R 4 is C 1 -C 10 alkyl.

9. The product of claim 2 wherein the chiral species has a structure selected from:

10. A method of fluorinating a nucleophilic substrate to form a fluorinated compound, the method comprising: contacting the substrate with a product as defined in claim 2 .

11. The product of 2 wherein R 4 is —CH 3 or CH 2 Cl.

12. The product of claim 2 , wherein the product is

or its enantiomer.

13. The product of claim 2 , wherein the product is

or its enantiomer.

14. The product of claim 2 , wherein the product is

or its enantiomer.

15. The product of claim 1 wherein R 4 is C 1 -C 10 alkyl.

16. The product of claim 1 wherein R 4 is —CH 3 or CH 2 Cl.

17. A method of fluorinating a nucleophilic substrate to form a fluorinated compound, the method comprising: contacting the substrate with a product as defined in claim 1 .

Assignees

• Univ Oxford Innovation Ltd

Inventors

• Gouverneur Veronique
• Sandford Graham

Classifications

• C07D487/08 Primary

  Bridged systems · CPC title

• C07B2200/07

  Optical isomers · CPC title

• C07C17/361

  by reactions involving a decrease in the number of carbon atoms · CPC title

• C07C2102/08

  Chemistry & Metallurgy · mapped topic

• C07C2103/40

  Chemistry & Metallurgy · mapped topic