Pentethylcyclanone

Chemical compound

"Cyclexanone" redirects here. For the organic compound, see Cyclohexanone.

Pharmaceutical compound

Pentethylcyclanone
Clinical data

Other names	Ciclexanona, cyclexanonum, cyclexanone
Identifiers
IUPAC name 2-(Cyclopenten-1-yl)-2-(2-morpholin-4-ylethyl)cyclopentan-1-one
CAS Number	15301-52-7 ^{[画像:check]Y}
PubChem CID	10355398
ChemSpider	8530850 ^{[画像:check]Y}
UNII	2OU4KS37EO
CompTox Dashboard (EPA)	DTXSID50934664 Edit this at Wikidata
Chemical and physical data
Formula	C₁₆H₂₅NO₂
Molar mass	263.381g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES C1CC=C(C1)C2(CCCC2=O)CCN3CCOCC3
InChI InChI=1S/C16H25NO2/c18-15-6-3-7-16(15,14-4-1-2-5-14)8-9-17-10-12-19-13-11-17/h4H,1-3,5-13H2^{[画像:check]Y} Key:KUOYUNPLUMKQIF-UHFFFAOYSA-N^{[画像:check]Y}

Pentethylcyclanone is an antitussive medication.^[1]

Synthesis

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Pentethylcyclanone can be prepared by alkylation of the anion of the self-condensation product of cyclopentanone with N-(2-chloroethyl)-morpholine.^[2]^[1]

Cyclexanone synthesis

References

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1 2 Dutta S, Bhat NS (December 2021). "Catalytic Transformation of Biomass-Derived Furfurals to Cyclopentanones and Their Derivatives: A Review". ACS Omega. 6 (51): 35145–35172. doi:10.1021/acsomega.1c05861 . PMC 8717399 . PMID 34984249.
↑ DE 1059901, Ueberwasser H, "Verfahren zur Herstellung von substituierten 2-Amino-alkylcycloalkanonen bzw, ihren Salzen [Process for the preparation of substituted 2-amino-alkylcycloalkanones or their salts]", published 1959年06月25日, assigned to Ciba AG