Hydroxyphenamate

Chemical compound From Wikipedia, the free encyclopedia

Hydroxyphenamate or oxyfenamate (trade name Listica) is a sedative and anxiolytic drug of the carbamate class which is no longer marketed in the US. Like other carbamate sedatives, it is chemically related to meprobamate (Miltown). It was introduced to the US market in 1961. The dosage for adults is 200 mg 3 to 4 times daily.[2]

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Hydroxyphenamate
Clinical data
Trade namesListica
Legal status
Legal status
Identifiers
  • (2-hydroxy-2-phenylbutyl) carbamate
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.000.016 Edit this at Wikidata
Chemical and physical data
FormulaC11H15NO3
Molar mass209.245 g·mol−1
3D model (JSmol)
  • CCC(COC(=O)N)(C1=CC=CC=C1)O
  • InChI=1S/C11H15NO3/c1-2-11(14,8-15-10(12)13)9-6-4-3-5-7-9/h3-7,14H,2,8H2,1H3,(H2,12,13)
  • Key:WAFIYOULDIWAKR-UHFFFAOYSA-N
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Synthesis

The reaction of propiophenone (1) with cyanide gives 2-hydroxy-2-phenylbutanenitrile (2).[3][4] Acid hydrolysis of the nitrile to a carboxylic acid gives 2-hydroxy-2-phenylbutanoic acid (3). The reduction by hydride of the acid to the alcohol gives 2-phenyl-1,2-butanediol (4). For the final step in the synthesis, treatment with ethyl chloroformate followed by addition of aqueous ammonia gave the carbamate, and hence hydroxyphenamate (5).

Synthesis of hydroxyphenamate

References

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