反応 #1269

ord-185abfaba55a4edabda0c165062f3325

反応方程式

COc1ccc(Cc2nccc3cc(OC)c(OC)cc23)cc1OC.Cl
Papaverine hydrochloride
COc1ccc(Cc2nccc3cc(OC)c(OC)cc23)cc1OC
papaverine
O=C(CBr)c1ccccc1
phenacyl bromide
c1ccc2c(c1)ccn1cccc21
pyrrolo[2,1-a]isoquinoline
収率 97.0%
Br.COc1ccc(Cc2nccc3cc(OC)c(OC)cc23)cc1OC
papaverine hydrobromide

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他to give 1 in 56% yield (Scheme 1)
  2. 2
    温度Refluxing the mixture for one hour
  3. 3
    その他produced good results
  4. 4
    温度additional heating

実験手順

A series of novel pyrrolo[2,1-a]isoquinoline dyes was prepared from readily available starting materials via a simple synthetic pathway. One such starting material is papaverine, a naturally occurring alkaloid that is relatively inexpensive and commercially available as its hydrochloride salt. Papaverine hydrochloride was converted to its free base in 97% yield. The free base was subsequently alkylated with phenacyl bromide in refluxing acetone to give 1 in 56% yield (Scheme 1). Refluxing the mixture for one hour produced good results; additional heating resulted in substantial decomposition of 1 to papaverine hydrobromide. Attempts to isolate 1 using benzene as solvent were unsuccessful. Sodium bicarbonate in water was mixed with 1 to give the cyclized product 2 in 82% yield. ##STR15##

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723617uspto-grants-1998_03