IP Library Granted Patent US 9,862,732
Granted Patent B2
US 9,862,732 · App. 14/961,472 · Granted Jan 9, 2018

Regioselective 1,2-dearomatization of functionalized azines by organolanthanide catalysts

Inventors: Tobin J. Marks (Evanston, IL); Massimiliano Delferro (Chicago, IL); Alexander S. Dudnik (Evanston, IL); Victoria L. Weidner (Evanston, IL)
Assignee: Northwestern University
C07F5/025B01J31/22C07F7/2212C07F17/00B01J2531/37
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Quick Facts
Patent No.
US 9,862,732
App. No.
14/961,472
Granted
Jan 9, 2018
Kind
B2
Abstract

A 1,2-regioselective organolanthanide-catalyzed azine dearomatization process using pinacolborane is disclosed.

Claims (41)

1. A method for dearomatizing an aromatic azine ring compound, said method comprising treating an azine ring compound comprising at least one nitrogen atom with at least one main-group element hydride in the presence of an organolathanide catalyst to afford a 1,2-dearomatized azine.

2. The method according to claim 1 , wherein the 1,2-dearomatized azine is regioselective.

3. The method according to claim 2 , wherein the regioselective 1,2-dearomatized azine is a regioselective 1,2-dihydropyridine.

4. A method according to claim 1 , wherein the at least one main-group element hydride is pinacolborane.

5. A method according to claim 1 , wherein the organolanthanide catalyst has a formula of (L) x Ln-H, wherein L is an ancillary ligand selected from a group consisting of Cp, Cp* and CGC, Cp″; Ln is a lanthanide element; X is an integer selected from a group consisting of 1 and 2; and H is hydrogen.

6. A method according to claim 5 , wherein the lanthanide element is selected from a group consisting of Sc, Y, La, Sm, Nd, Yb and Lu.

7. A method according to claim 1 , wherein the azine is a substituted with one or more subsituents.

8. A method according to claim 7 , wherein the one or more substituents are independently selected from a group consisting of halogen, CF 3 , OMe, (2S)-1-methyl-2-pyrrolidinyl, 1-piperidinyl, phenyl, vinyl, SnMe 3 , Bpin and fused ring systems and combinations thereof.

9. A method according to claim 1 , wherein the azine is pyridine.

10. A method according to claim 1 , wherein the azine and the at least one main-group element hydride are present in equimolar quantity.

11. A method according to claim 10 , wherein the catalyst is present in less than equimolar quantity relative to the azine and the at least one main-group element hydride.

12. A method according to claim 11 , wherein the catalyst is present in about 1% stoichiometric quantity relative to the azine and the at least one main-group element hydride.

13. A method according to claim 1 , wherein the treating of the azine with at least one main-group element hydride in the presence of an organolathanide catalyst is performed in a solvent comprising benzene.

14. A method according to claim 3 , wherein the regioselective 1,2-dihydropyridine is selected from a group consisting of:

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-phenyl-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-methyl-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-fluoro-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-methyl-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,5-methyl-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-methoxy-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydroquinoline;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydroisoquinoline;

1,4-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4-tetrahydropyrazine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-iodo-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-methoxy-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-piperidino-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-vinyl-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-trimethylstannyl-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-chloro-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-chloro-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-bromo-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-bromo-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-iodo-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-iodo-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-phenyl-1,2-dihydropyridine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-phenyl-1,2-dihydropylidine;

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-[(2S)-1-methyl-2-pyrrolidinyl-1,2-dihydropyridine; and

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-[(2S)-1-methyl-2-pyrrolidinyl-1,2-dihydropyridine (3s).

Assignments (3)
CONFIRMATORY LICENSE Recorded Sep 26, 2017
From: NORTHWESTERN UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 044005/0626 →
CONFIRMATORY LICENSE Recorded Mar 28, 2016
From: NORTHWESTERN UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 038274/0985 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 28, 2016
From: MARKS, TOBIN J.; DELFERRO, MASSIMILIANO; DUDNIK, ALEXANDR S.; WEIDNER, VICTORIA L.
To: NORTHWESTERN UNIVERSITY
Reel/Frame 037610/0339 →
Continuity (2)
Provisional Application 62088301 · Dec 5, 2014
Related Publication 20160159825A1 · Jun 9, 2016