تفاعل #46626

معادلة التفاعل

6-bromo-3-(2-methoxyethyl)-3,4-dihydro-1H-pyrido[2,3-d]pyrimidin-2-one

diisopropylethylamine

tri-ortho-tolylphosphine

N-(2-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide

→

title compound

المردود 36.0%

(E)-N-methyl-N-(2-methyl-1H-indol-3-ylmethyl)-3-[3-(2-methoxyethyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-6-yl]acrylamide

المردود 36.0%

المذيبات

propionitrile

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةwas heated
2. 2
   درجة الحرارةat reflux under N2 overnight
3. 3
   ترشيحThe dark mixture was filtered through a pad of Celite®
4. 4
   غسيلthe filter pad was rinsed with acetonitrile (250 mL)
5. 5
   تركيزThe filtrate was concentrated in vacuo
6. 6
   أخرىthe residue was purified by flash chromatography on silica gel (10% EtOAc/EtOH)

الإجراء التجريبي

A solution of 6-bromo-3-(2-methoxyethyl)-3,4-dihydro-1H-pyrido[2,3-d]pyrimidin-2-one (0.86 g, 3.00 mmole), N-(2-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide (see Example 1 (a), 0.68 g, 3.00 mmole), Pd(OAc)2 (0.07 g, 0.30 mmole), tri-ortho-tolylphosphine (0.18 g, 0.60 mmole) and diisopropylethylamine (1.31 mL, 7.50 mmole) in propionitrile (50 mL) was deoxygenated, then was heated at reflux under N2 overnight. The dark mixture was filtered through a pad of Celite®, and the filter pad was rinsed with acetonitrile (250 mL). The filtrate was concentrated in vacuo, and the residue was purified by flash chromatography on silica gel (10% EtOAc/EtOH). The title compound (0.46 g, 36%) was obtained as a light yellow solid after drying in vacuo: MS (ES) m/e 434 (M+H)+.

المصدر