Hydantoin

Hydantoin  |  |

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Names
Preferred IUPAC name

Imidazolidine-2,4-dione

Identifiers

CAS Number

* 461-72-3 Y

3D model (JSmol)

* Interactive image

ChEBI |

* CHEBI:27612 Y

ChEMBL |

* ChEMBL122334 Y

ChemSpider |

* 9612 Y

ECHA InfoCard | 100.006.650
KEGG |

* C05146 Y

PubChem CID

* 10006

UNII |

* I6208298TA

CompTox Dashboard (EPA)

* DTXSID1052111

InChI

* InChI=1S/C3H4N2O2/c6-2-1-4-3(7)5-2/h1H2,(H2,4,5,6,7) Y

Key: WJRBRSLFGCUECM-UHFFFAOYSA-N Y

* InChI=1/C3H4N2O2/c6-2-1-4-3(7)5-2/h1H2,(H2,4,5,6,7)

Key: WJRBRSLFGCUECM-UHFFFAOYAD

SMILES

* O=C1NC(=O)NC1

Properties

Chemical formula

| C3H4N2O2
Molar mass | 100.077 g·mol−1
Melting point | 220 °C (428 °F; 493 K)

Solubility in water

| 39.7 g/l (100 °C)

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Y verify (what is YN ?)

Infobox references

Chemical compound

Hydantoin, or glycolylurea, is a heterocyclic organic compound with the formula CH2C(O)NHC(O)NH. It is a colorless solid that arises from the reaction of glycolic acid and urea. It is an oxidized derivative of imidazolidine. In a more general sense, hydantoins can refer to groups or a class of compounds with the same ring structure as the parent compound. For example, phenytoin (mentioned below) has two phenyl groups substituted onto the number 5 carbon in a hydantoin molecule.[1]

## Synthesis

[edit]

Hydantoin was first isolated in 1861 by Adolf von Baeyer in the course of his study of uric acid. He obtained it by hydrogenation of allantoin, hence the name.

Friedrich Urech synthesized 5-methylhydantoin in 1873 from alanine sulfate and potassium cyanate in what is now known as the Urech hydantoin synthesis.[2] The method is very similar to the modern route using alkyl and arylcyanates. The 5,5-dimethyl compound can also be obtained from acetone cyanohydrin (also discovered by Urech: see cyanohydrin reaction) and ammonium carbonate.[3] This reaction type is called the Bucherer–Bergs reaction.[4][5]

Hydantoin can also be synthesized either by heating allantoin with hydroiodic acid or by "heating bromacetyl urea with alcoholic ammonia".[6] The cyclic structure of hydantoins was confirmed by Dorothy Hahn 1913.[7]

Of practical importance, hydantoins are obtained by condensation of a cyanohydrin with ammonium carbonate. Another useful route, which follows the work of Urech, involves the condensation of amino acids with cyanates and isocyanates:

## Uses and occurrence

[edit]

### Pharmaceuticals

[edit]

The hydantoin group can be found in several medicinally important compounds.[1] In pharmaceuticals, hydantoin derivatives form a class of anticonvulsants;[8] phenytoin and fosphenytoin both contain hydantoin moieties and are both used as anticonvulsants in the treatment of seizure disorders. The hydantoin derivative dantrolene is used as a muscle relaxant to treat malignant hyperthermia, neuroleptic malignant syndrome, spasticity, and ecstasy intoxication. Ropitoin is an example of an antiarrhythmic hydantoin.

### Pesticides

[edit]

The hydantoin derivative Imiprothrin is a pyrethroid insecticide. Iprodione is a popular fungicide containing the hydantoin group.[9]

### Synthesis of amino acids

[edit]

Hydrolysis of hydantoins affords amino acids:

RCHC(O)NHC(O)NH + H2O → RCHC(NH2)COOH + NH3

Hydantoin itself reacts with hot, dilute hydrochloric acid to give glycine. Methionine is produced industrially via the hydantoin obtained from methional.[9]

### Methylation

[edit]

Methylation of hydantoin yields a variety of derivatives. Dimethylhydantoin (DMH) [10] may refer to any dimethyl derivative of hydantoin, but especially 5,5-dimethylhydantoin.[11]

### Halogenation

[edit]

Some N-halogenated derivatives of hydantoin are used as chlorinating or brominating agents in disinfectant/sanitizer or biocide products. The three major N-halogenated derivatives are dichlorodimethylhydantoin (DCDMH), bromochlorodimethylhydantoin (BCDMH), and dibromodimethylhydantoin (DBDMH). A mixed ethyl-methyl analogue, 1,3-dichloro-5-ethyl-5-methylimidazolidine-2,4-dione (bromochloroethylmethylhydantoin), is also used in mixtures with the above.

Iprodione is a popular fungicide containing the hydantoin group.

### DNA oxidation to hydantoins after cell death

[edit]

A high proportion of cytosine and thymine bases in DNA are oxidized to hydantoins over time after the death of an organism. Such modifications block DNA polymerases and thus prevents PCR from working. Such damage is a problem when dealing with ancient DNA samples.[12]

## External links and further reading

[edit]

Look up dimethylhydantoin in Wiktionary, the free dictionary.

* Ware, Elinor (1950). "The Chemistry of the Hydantoins". Chem. Rev. 46 (3): 403–470\. doi:10.1021/cr60145a001. PMID 24537833.403-470&rft.date=1950&rft_id=info:doi/10.1021/cr60145a001&rft_id=info:pmid/24537833&rft.aulast=Ware&rft.aufirst=Elinor&rfr_id=info:sid/en.wikipedia.org:Hydantoin" class="Z3988">
* [1] Archived 2020-10-18 at the Wayback Machine English Translation of 1926 German review article on the Preparation of hydantoins by Heinrich Biltz and Karl Slotta

## References

[edit]

1. ^ a b Konnert, Laure; Lamaty, Frédéric; Martinez, Jean; Colacino, Evelina (2017). "Recent Advances in the Synthesis of Hydantoins: The State of the Art of a Valuable Scaffold" (PDF). Chemical Reviews. 117 (23): 13757–13809\. doi:10.1021/acs.chemrev.7b00067. PMID 28644621. S2CID 23653941.13757-13809&rft.date=2017&rft_id=https://api.semanticscholar.org/CorpusID:23653941#id-name=S2CID&rft_id=info:pmid/28644621&rft_id=info:doi/10.1021/acs.chemrev.7b00067&rft.aulast=Konnert&rft.aufirst=Laure&rft.au=Lamaty,+Frédéric&rft.au=Martinez,+Jean&rft.au=Colacino,+Evelina&rft_id=https://hal.archives-ouvertes.fr/hal-02385289/file/Hal-126.pdf&rfr_id=info:sid/en.wikipedia.org:Hydantoin" class="Z3988">
2. ^ Urech, Friedrich (1873). "Ueber Lacturaminsäure und Lactylharnstoff". Liebigs Ann. (in German). 165 (1): 99–103\. doi:10.1002/jlac.18731650110.99-103&rft.date=1873&rft_id=info:doi/10.1002/jlac.18731650110&rft.aulast=Urech&rft.aufirst=Friedrich&rft_id=https://zenodo.org/record/1427313&rfr_id=info:sid/en.wikipedia.org:Hydantoin" class="Z3988">
3. ^ Wagner, E. C.; Baizer, Manuel (1940). "5,5-Dimethylhydantoin". Organic Syntheses. 20: 42. doi:10.15227/orgsyn.020.0042; Collected Volumes, vol. 3, p. 323.
4. ^ Bucherer, H. T.; Steiner, W. (1934). "J. Prakt. Chem." (in German). 140: 291. `{{cite journal}}`: Cite journal requires `|journal=` (help)
5. ^ Bergs, Ger. pat. 566,094 (1929) [C. A., 27, 1001 (1933)].
6. ^ Chisholm, Hugh, ed. (1911). "Hydantoin" . Encyclopædia Britannica. Vol. 14 (11th ed.). Cambridge University Press. pp. 29–30.29-30&rft.edition=11th&rft.pub=Cambridge+University+Press&rft.date=1911&rfr_id=info:sid/en.wikipedia.org:Hydantoin" class="Z3988">
7. ^ Oakes, Elizabeth H. (2007). Encyclopedia of World Scientists. Facts on File. p. 298\. ISBN 9780816061587.
8. ^ "Hydantoin anticonvulsants". drugs.com.
9. ^ a b Drauz, Karlheinz; Grayson, Ian; Kleemann, Axel; Krimmer, Hans-Peter; Leuchtenberger, Wolfgang; Weckbecker, Christoph (2007). "Amino Acids". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a02_057.pub2. ISBN 978-3527306732.
10. ^ "5,5-Dimethylhydantoin (DMH) a Highly Effective, Halogen Stabilizer for Wet End Applications, PaperCo".
11. ^ "5,5-Dimethylhydantoin".
12. ^ Hofreiter, Michael; Serre, David; Poinar, Hendrik N.; Kuch, Melanie; Pääbo, Svante (2001). "Ancient DNA". Nature Reviews Genetics. 2 (5): 353–359\. doi:10.1038/35072071. PMID 11331901. S2CID 205016024.353-359&rft.date=2001&rft_id=https://api.semanticscholar.org/CorpusID:205016024#id-name=S2CID&rft_id=info:pmid/11331901&rft_id=info:doi/10.1038/35072071&rft.aulast=Hofreiter&rft.aufirst=Michael&rft.au=Serre,+David&rft.au=Poinar,+Hendrik+N.&rft.au=Kuch,+Melanie&rft.au=Pääbo,+Svante&rfr_id=info:sid/en.wikipedia.org:Hydantoin" class="Z3988">

* v
* t
* e

Anticonvulsants (N03)

GABAergics|

| GABAAR PAMs|

* Barbiturates: Barbexaclone
* Metharbital
* Methylphenobarbital
* Pentobarbital
* Phenobarbital#
* Primidone; Carbamates: Cenobamate
* Felbamate; Benzodiazepines: Clobazam
* Clonazepam
* Clorazepate
* Diazepam#
* Lorazepam#
* Midazolam
* Nimetazepam
* Nitrazepam
* Temazepam; Others: Bromide (potassium bromide, sodium bromide)
* Imepitoin
* Paraldehyde
* Stiripentol

|

GABA-T inhibitors|

* Fatty acids (and related): Valproate
* Valpromide
* Valproate pivoxil
* Vigabatrin

Others|

* GABAR agonists: Progabide; GAT-1 inhibitors: Tiagabine

Channel
modulators|

| Sodium blockers|

* Hydantoins: Ethotoin
* Fosphenytoin
* Mephenytoin
* Phenytoin#; Ureides: Acetylpheneturide
* Chlorphenacemide
* Phenacemide‡
* Pheneturide; Fatty acids: Valproate
* Valpromide
* Valproate pivoxil; Carboxamides:
* Carbamazepine#
* Eslicarbazepine acetate
* Oxcarbazepine; Others: Lacosamide
* Lamotrigine#
* Rufinamide
* Topiramate
* Zonisamide

|

Calcium blockers|

* Oxazolidinediones: Ethadione
* Paramethadione
* Trimethadione; Succinimides: Ethosuximide#
* Mesuximide
* Phensuximide; Gabapentinoids: Gabapentin
* Pregabalin; Others: Imepitoin
* Lamotrigine#
* Topiramate
* Zonisamide

Potassium openers|

* Retigabine

Others|

| CA inhibitors|

* Sulfonamides: Acetazolamide
* Ethoxzolamide
* Sultiame
* Topiramate
* Zonisamide

|

Others|

* Albutoin
* Beclamide
* Brivaracetam
* Cannabidiol
* Carisbamate
* Etiracetam
* Fenfluramine
* Ganaxolone
* Levetiracetam
* Perampanel

* #WHO-EM
* ‡Withdrawn from market
* Clinical trials:
* †Phase III
* §Never to phase III

*[CID]: Compound ID
*[EPA]: U.S. Environmental Protection Agency
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