Reaktion #1847362

Reaktionsgleichung

thionyl chloride

5-phenyl-1H-pyrazolo[4,3-c]isoquinoline-3-carboxylic acid

5-Phenyl-1H-pyrazolo[4,3-c]isoquinoline-3-carboxylic acid

sodium hydrogen carbonate

→

Methyl 5-phenyl-1H-pyrazolo[4,3-c]isoquinoline-3-carboxylate

Lösungsmittel

methanol

methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGThe mixture was stirred at RT for 12 h
2. 2
   Extraktionthe whole was extracted, in each case 1×, with ethyl acetate and methylene chloride
3. 3
   Trocknendried over magnesium sulfate
4. 4
   Einengenconcentrated under reduced pressure
5. 5
   Sonstigethe residue was purified by means of HPLC (Merk-Hibar-Lichrospher 100-RP-18, water (0.1% trifluoroacetic acid)/acetonitrile (0.1% trifluoroacetic acid)=80/20→10/90)
6. 6
   SonstigeThe following was obtained

Vorschrift

18 μL of thionyl chloride were initially introduced into 0.5 ml of methanol and the mixture was stirred for 30 min. 19 mg of 5-phenyl-1H-pyrazolo[4,3-c]isoquinoline-3-carboxylic acid (60) in 0.5 ml of methanol were then added dropwise. The mixture was stirred at RT for 12 h, after which a saturated solution of sodium hydrogen carbonate was added and the whole was extracted, in each case 1×, with ethyl acetate and methylene chloride. The organic phases were combined, dried over magnesium sulfate and concentrated under reduced pressure and the residue was purified by means of HPLC (Merk-Hibar-Lichrospher 100-RP-18, water (0.1% trifluoroacetic acid)/acetonitrile (0.1% trifluoroacetic acid)=80/20→10/90). The following was obtained: 61. C18H13N3O2 (303.32) MS (ESI) 304 (M+H)

Quelle