반응 #3271

ord-dc089cf7000c4b12a70b5ffd130e6b36

반응 방정식

Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(O)nc2n1
2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one
Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(O)nc2n1
2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7-ol
[H-].[Na+]
NaH
CCI
Ethyl iodide
CCn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(N)nc21
2-amino-6-(2,6-dichlorophenyl)-8-ethyl-pyrido[2,3-d]pyrimidin-7(8H)-one
수율 55.4%

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타resulting in a clear solution
  2. 2
    온도cooled to room temperature
  3. 3
    기타The resulting precipitate was removed by filtration
  4. 4
    기타partitioned between ethyl acetate and water
  5. 5
    기타The organic layer was separated
  6. 6
    건조dried over MgSO4
  7. 7
    여과filtered
  8. 8
    농축concentrated in vacuo
  9. 9
    세척Flash chromatography, eluting with ethyl acetate

실험 절차

To a suspension of NaH (60% in mineral oil, 27 mg) in 5 mL of dimethylformamide was added 2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one (172 mg, 0.56 mmol) from Example 11. The mixture was heated at 50° C. for 1 hour resulting in a clear solution. Ethyl iodide (60 μL, 0.75 mmol) was added, and the solution was stirred at 50° C. for 3.5 hours, cooled to room temperature, and poured into 30 mL of ice water. The resulting precipitate was removed by filtration and partitioned between ethyl acetate and water. The organic layer was separated and dried over MgSO4, filtered, and concentrated in vacuo. Flash chromatography, eluting with ethyl acetate, provided 104 mg (55%) of 2-amino-6-(2,6-dichlorophenyl)-8-ethyl-pyrido[2,3-d]pyrimidin-7(8H)-one; mp 207°-209° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733914uspto-grants-1998_03