Réaction #82966

ord-7ea080331a9f4b34b887931f635af00e

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe mixture was heated under an argon gas stream for 24 hours
  2. 2
    TempératureAfter the reaction solution was cooled
  3. 3
    Autrethe crystals which separated out
  4. 4
    Filtrationwere collected by filtration

Mode opératoire

(i) To 1.15 g of (R)-(+)-N-acetyl-7,8-dihydroxy-4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline 1/4 hydrate were added 9 ml of 3N hydrochloric acid and 9 ml of ethanol, and the mixture was heated under an argon gas stream for 24 hours. After the reaction solution was cooled, the crystals which separated out were collected by filtration, affording 1.09 g of (R)-(+)-7,8-dihydroxy-4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride monohydrate.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05623074uspto-grants-1997_04