Reaction #452476

ord-568fb293b9284b7c90b0164facd81129

Reaction equation

O=C[O-].[NH4+]
Ammonium formate
c1ccc(CN2CCN(c3nccc4ccccc34)CC2)cc1
product
c1ccc(CN2CCN(c3nccc4ccccc34)CC2)cc1
1-[4-Benzyl-(1-piperazinyl)]isoquinoline
c1ccc2c(N3CCNCC3)nccc2c1
product
c1ccc2c(N3CCNCC3)nccc2c1
1-[1-Piperazinyl]isoquinoline

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturewas heated at 75° C. for 16 h
  2. 2
    Filtrationthe mixture filtered through Kieselguhr
  3. 3
    Concentrationconcentrated in vacuo

Procedure

Ammonium formate (1.01 g, 16.0 mmol) and 10% Pd/C 42.5 mg, 0.4 mmol, 10 mol%) were added successively to a stirred solution of the product of Example 21 (1.23 g, 4.06 mmol) in methanol (4 ml). The mixture was stirred at room temperature for 6 h and was heated at 75° C. for 16 h. Methanol (40 ml) was added and the mixture filtered through Kieselguhr, and concentrated in vacuo to give the product as a pale yellow oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06127357uspto-grants-2000_10