반응 #8819

ord-b8fb1c319e5948b89f7e69697197210e

반응 방정식

Cc1cccc(-n2cnc3c2CCN(Cc2ccccc2)C3)c1
5-benzyl-1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine
O=C[O-].[NH4+]
ammonium formate
Cc1cccc(-n2cnc3c2CCNC3)c1
1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine
수율 32.2%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도at reflux for 12 hr
  3. 3
    기타to reach ambient temperature
  4. 4
    기타The catalyst was removed by filtration through Celite®
  5. 5
    기타The filtrate was evaporated in vacuo
  6. 6
    기타Purification by silica gel chromatography

실험 절차

A mixture of 5-benzyl-1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine 17a (500 mg, 1.6 mmol), ammonium formate (1.0 g), and 700 mg 5% Pd/C (50% with water) in 80% aqueous methanol was heated at reflux for 12 hr, and then allowed to reach ambient temperature. The catalyst was removed by filtration through Celite®. The filtrate was evaporated in vacuo. Purification by silica gel chromatography provided 1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine (110 mg) 18a as an oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091200B2uspto-grants-2006_08