Feclemine

Feclemine
	File:Feclemine.svg
Clinical data
Other names	Fenetamin; Giacosil; Licabile; Licaran; Phenecyclamine; Phenetamine; Spasmexan; UCB-1545;
Identifiers
	IUPAC name 2-[Cyclohexyl(phenyl)methyl]-N,N,N',N'-tetraethylpropane-1,3-diamine;
CAS Number	3590-16-7;
PubChem CID	3030835;
ChemSpider	2295996;
UNII	5P7U986QGO;
ChEBI	CHEBI:135518;
ChEMBL	ChEMBL2106137;
PDB ligand	PD072576 (PDBe, RCSB PDB);
E number	{{#property:P628}}
CompTox Dashboard (EPA)	DTXSID80863211;
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C24H42N2
Molar mass	358.614 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCN(CC)CC(CN(CC)CC)C(C1CCCCC1)C2=CC=CC=C2;
	InChI InChI=1S/C24H42N2/c1-5-25(6-2)19-23(20-26(7-3)8-4)24(21-15-11-9-12-16-21)22-17-13-10-14-18-22/h9,11-12,15-16,22-24H,5-8,10,13-14,17-20H2,1-4H3; Key:QDMORDTWFMWOFA-UHFFFAOYSA-N;

Feclemine (phenetamine) is a spasmolytic drug.^[1]

Synthesis

The chemical synthesis is discussed:^[2]

File:Feclemine synthesis.svg

Sodamide is used to alkylate cyclohexylphenylacetonitrile [3893-23-0] (1) (also used for drofenine) with 2-chloro-N,N,N',N'-tetraethylpropane-1,3-diamine [3492-54-4] (HCl: [94465-65-3]) to give (2). Some rearrangement is possible to give a mixture of regioisomers. Sodamide catalyzed cleavage of the nitrile group in a separate step then completes the synthesis of feclemine (3).

File:Feclemine sidechain synthesis.svg

Precursor:^[3] Alcohol:^[3]

References

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[1]

[2]

[3]

Clinical data
File:Feclemine.svg
Other names	Fenetamin Giacosil Licabile Licaran Phenecyclamine Phenetamine Spasmexan UCB-1545
Identifiers
IUPAC name 2-[Cyclohexyl(phenyl)methyl]-N,N,N',N'-tetraethylpropane-1,3-diamine
CAS Number	3590-16-7
PubChem CID	3030835
ChemSpider	2295996
UNII	5P7U986QGO
ChEBI	CHEBI:135518
ChEMBL	ChEMBL2106137
PDB ligand	PD072576 (PDBe, RCSB PDB)
E number	{{#property:P628}}
CompTox Dashboard (EPA)	DTXSID80863211
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C₂₄H₄₂N₂
Molar mass	358.614 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES CCN(CC)CC(CN(CC)CC)C(C1CCCCC1)C2=CC=CC=C2
InChI InChI=1S/C24H42N2/c1-5-25(6-2)19-23(20-26(7-3)8-4)24(21-15-11-9-12-16-21)22-17-13-10-14-18-22/h9,11-12,15-16,22-24H,5-8,10,13-14,17-20H2,1-4H3 Key:QDMORDTWFMWOFA-UHFFFAOYSA-N

Feclemine

Synthesis

References

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