IP Library Granted Patent US 9,701,684
Granted Patent B2
US 9,701,684 · App. 14/440,530 · Granted Jul 11, 2017

Chiral fluorinating reagents

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Quick Facts
Patent No.
US 9,701,684
App. No.
14/440,530
Granted
Jul 11, 2017
Kind
B2
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.

Claims (43)

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 .

Assignments (2)
CHANGE OF NAME Recorded Aug 2, 2016
From: ISIS INNOVATION LIMITED
To: OXFORD UNIVERSITY INNOVATION LIMITED
Reel/Frame 039550/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2015
From: GOUVERNEUR, VERONIQUE; SANDFORD, GRAHAM
To: ISIS INNOVATION LIMITED
Reel/Frame 036160/0323 →