تفاعل #46486

ord-084ea8b076b0498e837cf0a5106a25e5

معادلة التفاعل

Nc1ccc(Br)cn1
2-amino-5-bromopyridine
C=CC(=O)OCc1ccccc1
benzyl acrylate
Cc1ccccc1P(c1ccccc1C)c1ccccc1C
tri-ortho-tolylphosphine
CCN(C(C)C)C(C)C
diisopropylethylamine
Nc1ccc(/C=C/C(=O)OCc2ccccc2)cn1
title compound
المردود 39.3%
Nc1ccc(/C=C/C(=O)OCc2ccccc2)cn1
Benzyl (E)-3-(6-aminopyridin-3-yl)acrylate
المردود 39.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux overnight
  2. 2
    ترشيحThe dark mixture was filtered through Celite®
  3. 3
    تركيزthe filtrate was concentrated

الإجراء التجريبي

A solution of 2-amino-5-bromopyridine (2.25 g, 13.0 mmole), benzyl acrylate (3.2 g, 19.7 mmole), Pd(OAc)2 (0.31 g, 1.4 mmole), tri-ortho-tolylphosphine (0.73 g, 2.4 mmole), and diisopropylethylamine (3.5 mL, 20.0 mmole) in propionitrile (50 mL) was heated at reflux overnight. The dark mixture was filtered through Celite®, and the filtrate was concentrated. Flash chromatography on silica gel (3% MeOH/CH2Cl2) gave the title compound (1.3 g, 39%): MS (ES) m/e 255 (M+H)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07741339B2uspto-grants-2010_06