반응 #6625
ord-f4b94ff8ba9e4c06ac8d51b313e46253
반응 방정식
반응물
반응 조건
후처리
- 1온도is heated
- 2온도at reflux under nitrogen
- 3온도the reaction mixture is heated
- 4온도at reflux under nitrogen for an additional 12 hours
- 5농축The reaction mixture then is concentrated under reduced pressure
- 6기타the residue chromatographed on silica gel
- 7세척eluting 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
- 10여과The solid which forms is collected by filtration
- 11세척washed with cold ethyl acetate
- 12기타dried
실험 절차
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.