Aminoketone
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Aminoaldehydes and aminoketones are
organic compound In chemistry, organic compounds are generally any chemical compounds that contain carbon-hydrogen or carbon-carbon bonds. Due to carbon's ability to catenate (form chains with other carbon atoms), millions of organic compounds are known. The ...
s that contain an
amine In chemistry, amines (, ) are compounds and functional groups that contain a basic nitrogen atom with a lone pair. Amines are formally derivatives of ammonia (), wherein one or more hydrogen atoms have been replaced by a substituen ...
functional group as well as either a
aldehyde In organic chemistry, an aldehyde () is an organic compound containing a functional group with the structure . The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl grou ...
or
ketone In organic chemistry, a ketone is a functional group with the structure R–C(=O)–R', where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group –C(=O)– (which contains a carbon-oxygen double bo ...
functional group. These compounds are important in biology and in chemical synthesis. Because of their bifunctional nature, they have attracted much attention from chemists.


Tertiary amine derivatives

Because primary and secondary amines react with aldehydes and ketones, the most common variety of these aminocarbonyl compounds feature tertiary amines. Such compounds are produced by amination of α- haloketones and α- haloaldehydes. Examples include
cathinone Cathinone (also known as benzoylethanamine, or β-keto-amphetamine) is a monoamine alkaloid found in the shrub '' Catha edulis'' (khat) and is chemically similar to ephedrine, cathine, methcathinone and other amphetamines. It is probably the m ...
s, methadone,
molindone Molindone, sold under the brand name Moban, is an antipsychotic which is used in the United States in the treatment of schizophrenia. It works by blocking the effects of dopamine in the brain, leading to diminished symptoms of psychosis. It is r ...
, pimeclone, ferruginine, and
tropinone Tropinone is an alkaloid, famously synthesised in 1917 by Robert Robinson as a synthetic precursor to atropine, a scarce commodity during World War I. Tropinone and the alkaloids cocaine and atropine all share the same tropane core structure. I ...
.


Secondary amine derivatives

Aminoketones containing secondary amines are typically stable when the ketone is located on a ring, e.g.
4-piperidinone 4-Piperidinone is a derivative of piperidine with the molecular formula C5 H9 N O. 4-Piperidone is used as an intermediate in the manufacture of chemicals and pharmaceutical drugs. Piperidones Piperidones are a class of chemical compounds sharin ...
, triacetonamine, acridone


Primary amine derivatives

Most members of this class are unstable towards self-condensation, however some important examples do exist as intermediates in biosynthetic pathways e.g.
glutamate-1-semialdehyde Glutamate-1-semialdehyde is a molecule formed from by the reduction of tRNA bound glutamate, catalyzed by glutamyl-tRNA reductase. It is isomerized by glutamate-1-semialdehyde 2,1-aminomutase to give aminolevulinic acid in the biosynthesis of por ...
. The acyclic forms of certain
amino sugar In organic chemistry, an amino sugar (or more technically a 2-amino-2-deoxysugar) is a sugar molecule in which a hydroxyl group has been replaced with an amine group. More than 60 amino sugars are known, with one of the most abundant being ''N'' ...
s also qualify, for instance
vancosamine Vancosamines are aminosugars that are a part of vancomycin and other molecules within the vancomycin family of antibiotics. Vancosamine synthesis is encoded by the vancomycin (''vps'') biosynthetic cluster. Epivancosamine, a closely related amino ...
.
Aminoacetaldehyde Aminoacetaldehyde is the organic compound with the formula OHCCH2NH2. Under the usual laboratory conditions, it is unstable, tending instead to undergo self-condensation. Aminoacetaldehyde diethylacetal is a stable surrogate. In nature, aminoac ...
, the simplest member of this subclass, is highly reactive toward self-condensation.
Aminoacetaldehyde diethylacetal Aminoacetaldehyde diethylacetal is the organic compound with the formula (EtO)2CHCH2NH2. A colorless liquid, it is used as a surrogate for aminoacetaldehyde. See also * Aminoaldehydes and aminoketones Aminoaldehydes and aminoketones are organic ...
, (EtO)2CHCH2NH2, is a stable analogue that is commercially available.
2-Aminobenzaldehyde 2-Aminobenzaldehyde is an organic compound with the formula C6H4(NH2)CHO. It is one of three isomers of aminobenzaldehyde. It is a low-melting yellow solid that is soluble in water. Preparation and reactions It is usually prepared by reduction ...
with the formula C6H4(NH2)CHO is a prominent aromatic aminoaldehyde. The compound is unstable with respect to self-condensation
Aminoacetone Aminoacetone is the simplest monopeptide with the formula CH3C(O)CH2NH2. Although stable in the gaseous form, once condensed it reacts with itself. The protonated derivative forms stable salts, e.g. aminoacetone hydrochloride ( H3C(O)CH2NH3l)). ...
is a prominent member of this class of compounds. It is unstable under normal laboratory conditions, but the hydrochloride H3C(O)CH2NH3l is readily isolable. Aminoacetone is derived from decarboxylation of alanine. Aminoacetaldehyde is produced by the hydroxylation of taurine.


References

{{organic-compound-stub Amines Ketones Aldehydes