Process for preparing amino compounds by using salen-manganese complexes as the catalyst
AssigneeJapan Science and Technology Corporation
InventorsTsutomu Katsuki, Yoshinori Kohmura
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Abstract
Disclosed is a process for the enantioselective production of an optically active amino compound by the amination of the C—H bond of an organic compound. The amino compound is produced by converting the C—H bond at the allyl position of an alkene or the C—H bond at the benzyl position of an alkylarene to the corresponding C—N bond, using a salen-manganese complex as the catalyst and N-substituted iminoaryliodinane as the amination agent. Both the catalytic activity and the enantioselectivity are very high when there is used a catalyst in which the 3- and 5-positions of the salicylaldehyde moiety of the salen ligand are substituted with an electron-withdrawing group, particularly with a halogen atom.
Claims6
A process for producing an amino compound from an alkene or from an alkylarene, which comprises converting the C—H bond at the allyl position of the alkene or the C—H bond at the benzyl position of the alkylarene, to the C—N bond, wherein there are used an optically active salen-manganese complex as the catalyst and a N-substituted iminoaryliodinane as the amination agent, the optically active salen-manganese complex being expressed by formula (1):
- in which at least one of R1 and R2 denotes an electron-withdrawing group, and R3 denotes an alkyl group having 1 to 4 carbon atoms, a phenyl group, or a group in which the two R3's are linked together to form a five- to seven-membered alicyclic hydrocarbon group.
Dependencies are inferred from the claim text.