Sulfonamide-based organocatalysts and method for their use
View Patent ↗Organocatalysts, particularly proline sulfonamide organocatalysts, having a first general formula as follows are disclosed. Embodiments of a method for using these organocatalysts also are disclosed. The method comprises providing a disclosed organocatalyst, and performing a reaction, often an enantioselective or diastereoselective reaction, using the organocatalyst. Solely by way of example, disclosed catalysts can be used to perform aldol reactions, conjugate additions, Michael additions, Robinson annulations, Mannich reactions, α-aminooxylations, α-hydroxyaminations, α-aminations and alkylation reactions. Certain of such reactions are intramolecular cyclizations used to form cyclic compounds, such as 5-or 6-membered rings, having one or more chiral centers Disclosed organocatalysts generally are much more soluble in typical solvents used for organic synthesis than are known compounds. Moreover, the reaction yield is generally quite good with disclosed compounds, as is their enantioselective and diastereoselective effectiveness.
1. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a formula
where R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl: n is from 1-5; and each of the aliphatic substituents as 4 or more carbon atoms.
2. The catalyst according to claim 1 having formula
where n is from 8-24.
3. The catalyst according to claim 1 having formula
4. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
where R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl: and R 15 and R 16 are alkyl comprising 4 or more carbon atoms.
5. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
where R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl; and n is from 1 to 5.
6. The catalyst according to claim 5 where at least one ester is an alkyl ester having from 4 to 24 carbon atoms.
7. The catalyst according to claim 5 where at least one ester is p-dodecyl ester.
8. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
where R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl: and n is from 1 to 5.
9. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
where R 1 , R 2 , R 4 , and R 5 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or a polymer support; R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl: and R 21 -R 25 are independently selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl aryl alkyl, substituted aryl alkyl, cyclic, substituted cyclic, ester, ether, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, silyl, or are bonded together to form a ring.
10. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
where R 1 , R 2 , and R 5 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or a polymer support; R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl: R 17 -R 20 are independently selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, cyclic, substituted cyclic, ester, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, hydrogen, hydroxyl, ketone, nitro, nitroso, or are bonded together to form a ring; and where at least one of R 1 , R 2 , R 5 -R 14 , and R 17 -R 20 is other than hydrogen.
11. The catalyst according to claim 10 where R 1 -R 2 , R 5 and R 17 -R 20 independently are alkyl, hydrogen or halogen.
12. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
where R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl: n is from 1 to 5; and at least one ether functional group comprises 4 or more carbon atoms and is aliphatic, substituted aliphatic, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, cyclic, substituted cyclic, heterocyclic or substituted hetereocyclic.
13. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
where R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl: X is a halogen; and R 3 -R 5 are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, cyclic, substituted cyclic, ester, ether, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, or silyl.
14. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
15. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a structure
where R 6 -R 11 independently are selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, pyrrolidine, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; R 12 -R 14 are independently selected from hydrogen and lower alkyl; n is from 1 to 5; and at least one ketone has 4 or more carbon atoms.
16. The catalyst according to claim 1 having a formula
where R 8 is selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, azide, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or is an atom in a ring.
17. A catalyst for making compounds having an enantiomeric excess of at least about 70%, the catalyst having a formula
where R 1 -R 5 are independently selected from aliphatic, substituted aliphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are bonded together to form a ring; at least one of such substitutes comprise 4 or more carbon atoms, at least one of R 1 and R 5 is hydrogen or halogen, and if R 1 -R 5 is aryl, the aryl group is directly bonded to a carbon atom bearing one of R 1 -R 5 ; R 6 -R 7 independently are selected from aliphatic and hydrogen; R 8 is selected from substitutes defining naturally occurring amino acids; R 9 -R 10 are independently aliphatic, or hydrogen; and R 11 and R 12 are independently selected from alphatic, substituted alphatic, alkoxy, substituted alkoxy, amine, substituted amine, amide, substituted amide, aryl, substituted aryl, aryl alkyl, substituted aryl alkyl, cyclic, substituted cyclic, ester, ether, formyl, halogen, heterocyclic, substituted heterocyclic, heteroaryl, substituted heteroaryl, hydrogen, hydroxyl, ketone, substituted ketone, nitro, nitroso, protecting groups, silyl, silyl ether, silyl ester, thiol, thiol ether, thiol ester, or are atoms in a ring.
18. The catalyst according to claim 17 having a formula
where each R is selected from hydrogen, lower alkyl, carbamate, acyl, or silyl.
19. The catalyst according to claim 5 having a structure