Carfenazine

Carfenazine

Clinical data
Other names	Proketazine, Carphenazin
License data	US FDA: Proketazine
Routes of administration	Oral
ATC code	none
Legal status
Legal status	Withdrawn
Identifiers
IUPAC name 1-(10-{3-[4-(2-Hydroxyethyl)piperazin-1-yl]propyl}-10H-phenothiazin-2-yl)propan-1-one
CAS Number	2622-30-2
PubChem CID	18104
IUPHAR/BPS	7140
DrugBank	DB01038
ChemSpider	17100
UNII	CLY16Y8Z7E
ChEBI	CHEBI:51235
ChEMBL	ChEMBL1201328
CompTox Dashboard (EPA)	DTXSID8022745
ECHA InfoCard	100.018.249
Chemical and physical data
Formula	C24H31N3O2S
Molar mass	425.59 g·mol−1
3D model (JSmol)	Interactive image
SMILES CCC(=O)c1ccc2Sc3ccccc3N(CCCN4CCN(CCO)CC4)c2c1
InChI InChI=1S/C24H31N3O2S/c1-2-22(29)19-8-9-24-21(18-19)27(20-6-3-4-7-23(20)30-24)11-5-10-25-12-14-26(15-13-25)16-17-28/h3-4,6-9,18,28H,2,5,10-17H2,1H3 Key:XZSMZRXAEFNJCU-UHFFFAOYSA-N

Carfenazine (INN) (former developmental code name WY-2445), or carphenazine (BAN), also known as carphenazine maleate (USAN) (brand name Proketazine; former developmental code name NSC-71755), is an antipsychotic and tranquilizer of the phenothiazine group that was withdrawn from the market.

Synthesis

Thieme Synthesis: Patent:

The alkylation reaction between 2-Propionyl Phenothiazine [92-33-1] (1) and 1-Bromo-3-chloropropane (2) gives 1-[10-(3-chloropropyl)phenothiazin-2-yl]propan-1-one [95157-45-2] (3). A second alkylation step, this time with 2-(1-Piperazinyl)ethanol [103-76-4] (4) completes the synthesis of Carfenazine (5).

NB: Although above procedure is proof-of-concept, bear in mind no protecting group {Other patent uses ketalization technique}

Analogues

• Butaperazine uses butanoyl (Butyryl) and not propanoyl group.
• Fluphenazine selfsame but trifluoromethyl on position 2 of the phenothiazine ring.