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US 11,584,720 B2Granted
Photoredox-catalyzed direct C-H functionalization of arenes
AssigneeThe University of North Carolina at Chapel Hill
InventorsDavid Nicewicz, Nathan Romero, Kaila Margrey, Nicholas Tay
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Abstract
The invention generally relates to methods of making substituted arenes via direct C—H amination. More specifically, methods of making para- and ortho-substituted arenes via direct C—H amination are disclosed. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
Claims23
A method of making a compound having a structure represented by a formula:
- wherein E is an electron donating group;
- wherein each of Q1 and Q3 is independently selected from N and CR1;
- wherein each of Q2 and Q4 is independently selected from N and CR2;
- wherein each occurrence of R1 and R2 is independently selected from hydrogen, halogen, C1-C8 alkyl, C1-C8 alkoxy, and —C(═O)NR3aR3b;
- or
- wherein R1 and R2 are optionally covalently bonded and, together with the intermediate atoms, form a 5- to 6-membered cycle or heterocycle having 0, 1, or 2 heteroatoms, and are substituted with 0, 1, 2, or 3 groups independently selected from halogen, C1-C8 alkyl, C1-C8 alkoxy, and —C(═O)NR3aR3b;
- wherein each of R3a and R3b is independently selected from hydrogen and C1-C4 alkyl;
- wherein Z is selected from 18F and —CN,
- the method comprising the steps of:
- (a) reacting a compound having a structure represented by a formula:
- with a nucleophile selected from a 18F-labeled fluoride and a cyanide, in the presence of a catalytically effective amount of an acridinium photocatalyst;
- and
- (b) reacting with an oxidant.
10 more elements
Dependencies are inferred from the claim text.