반응 #6625

ord-f4b94ff8ba9e4c06ac8d51b313e46253

반응 방정식

CC(C)(C)C(=O)Nc1cc2c(O)n(C=CCOC3CCCCO3)cnc-2n1
3-(3-tetrahydropyr-2-yloxyprop-1-en-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine
CCOC(=O)CC[C@H](NC(=O)c1ccc(I)cc1)C(=O)OCC
diethyl N-(4-iodobenzoyl)glutamate
Cc1ccccc1P(c1ccccc1C)c1ccccc1C
tris-(2-methylphenyl)phosphine
CCOC(=O)[C@H](CCC(=O)[O-])NC(=O)c1ccc(I)cc1
ethyl N-(4-iodobenzoyl)glutamate
CCOC(=O)CC[C@H](NC(=O)c1ccc(C(=Cn2cnc3nc(NC(=O)C(C)(C)C)cc-3c2O)COC2CCCCO2)cc1)C(=O)OCC
diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도is heated
  2. 2
    온도at reflux under nitrogen
  3. 3
    온도the reaction mixture is heated
  4. 4
    온도at reflux under nitrogen for an additional 12 hours
  5. 5
    농축The reaction mixture then is concentrated under reduced pressure
  6. 6
    기타the residue chromatographed on silica gel
  7. 7
    세척eluting with 20:1 ethyl acetate
  8. 8
    workup.DISSOLUTION) The concentrated material is dissolved in 1:5 ethyl acetate
  9. 9
    workup.WAITether and this solution is refrigerated for 15 hours
  10. 10
    여과The solid which forms is collected by filtration
  11. 11
    세척washed with cold ethyl acetate
  12. 12
    기타dried

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05248775uspto-grants-1993_09