Reaction #6625
ord-f4b94ff8ba9e4c06ac8d51b313e46253
Reaction equation
Reactants
Reagents
Solvents
Conditions
Workup
- 1Temperatureis heated
- 2Temperatureat reflux under nitrogen
- 3Temperaturethe reaction mixture is heated
- 4Temperatureat reflux under nitrogen for an additional 12 hours
- 5ConcentrationThe reaction mixture then is concentrated under reduced pressure
- 6Otherthe residue chromatographed on silica gel
- 7Washeluting with 20:1 ethyl acetate
- 8workup.DISSOLUTION) The concentrated material is dissolved in 1:5 ethyl acetate
- 9workup.WAITether and this solution is refrigerated for 15 hours
- 10FiltrationThe solid which forms is collected by filtration
- 11Washwashed with cold ethyl acetate
- 12Otherdried
Procedure
A mixture containing 3.48 g of 3-(3-tetrahydropyr-2-yloxyprop-1-en-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine, 3.12g (1.2 equiv.) of diethyl N-(4-iodobenzoyl)glutamate, 546 mg (20%) of tris-(2-methylphenyl)phosphine, 201 mg (10%) of palladium acetate and 85.5 mg (5%) of cuprous iodide in 15 ml of triethylamine and 240 ml of acetonitrile is heated at reflux under nitrogen. After 12 hours., 1.17 g of ethyl N-(4-iodobenzoyl)glutamate are added and the reaction mixture is heated at reflux under nitrogen for an additional 12 hours. The reaction mixture then is concentrated under reduced pressure and the residue chromatographed on silica gel, eluting with 20:1 ethyl acetate:hexane. (Any recovered starting material can be recycled through the foregoing procedure.) The concentrated material is dissolved in 1:5 ethyl acetate:ether and this solution is refrigerated for 15 hours. The solid which forms is collected by filtration, washed with cold ethyl acetate and dried to yield diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate.