تفاعل #684968

ord-d558389e953e49db9fe05adf4d1eabfa

معادلة التفاعل

Nc1cccnc1Cl
2-chloro-3-aminopyridine
C1CCOC1
tetrahydrofuran
CCOC(C)=O
ethyl acetate
Cln1ccc2ncccc21
1-chloropyrrolopyridine
CCCCc1ccc(Cc2nccc3cc[nH]c23)cc1
title compound
CCCCc1ccc(Cc2nccc3cc[nH]c23)cc1
7-(4-Butylbenzyl)-1H-pyrrolo[2,3-c]pyridine

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooling
  2. 2
    درجة الحرارةwhile heating
  3. 3
    درجة الحرارةunder reflux for 4 hours
  4. 4
    غسيلThe resulting mixture was washed with a saturated aqueous ammonium chloride solution and saturated brine
  5. 5
    تركيزconcentrated under reduced pressure
  6. 6
    أخرىThe residue was purified by silica gel column chromatography

الإجراء التجريبي

The compound of Example B205 (800 μl, 0.3 mmol) was added to a solution of 1-chloropyrrolopyridine (19.4 mg, 0.127 mmol), which was synthesized from 2-chloro-3-aminopyridine according to the method of H07-165,708A, and dichloro(diphenylphosphinopropane)nickel (6.9 mg, 0.013 mmol) in tetrahydrofuran (1 ml) under ice-cooling, and the mixture was stirred while heating under reflux for 4 hours. After allowing the mixture to cool to room temperature, ethyl acetate was added thereto. The resulting mixture was washed with a saturated aqueous ammonium chloride solution and saturated brine, then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (7.1 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897387B2uspto-grants-2011_03