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Tetrahydrofuran → Diethylether ethylacetate

HRID 257789
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HRID 257789 반응식
ClC1C=C(C=CC=1)NC1C(CN)=CC=CN=1.C(N1C=CN=C1)(N1C=CN=C1)=[O:18].ClC1C=C(N2C3N=CC=CC=3CNC2=O)C=CC=1.[O:47]1[CH2:51][CH2:50][CH2:49][CH2:48]1>>[C:48]([O:47][CH2:51][CH3:50])(=[O:18])[CH3:49].[CH2:48]([O:47][CH2:51][CH3:50])[CH3:49]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 8028TetrahydrofuranHCID 682631,1'-CarbonyldiimidazoleHCID 132592941-(3-Chlorophenyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-oneHCID 19781588HCID 19781588, 화합물

생성물 1

HCID 21584169Diethylether ethylacetate수율 50%

실험 절차

Sodium hydride (previously washed in hexanes) was added to a solution of 2-(3-chloroanilino)-3-aminomethylpyridine (10.3 g, 44.1 mmole) in tetrahydrofuran (200 ml). The solution was stirred at room temperature for 5 minutes. 1,1'-Carbonyldiimidazole (10.7 g, 66.1 mmole) was added gradually to the solution with stirring; after the addition the solution was refluxed for 22 hours. The solvents were removed and H2O was added to the residue. The solid material was extracted in ethyl acetate, washed with H2O and dried over MgSO4. The MgSO4 was removed by filtration and the solvents by evaporation. The product was recrystallized out of ethyl acetate/ethyl ether yielding 5.7 g (21.9 mmole, 50% yield) of 1-(3-chlorophenyl)pyrido[2,3-d]pyrimidine-2(1H,3H)-one (mp 188°-187° C.), as a tan solid.

후처리

  1. washSodium hydride (previously washed in hexanes)
  2. stirringwith stirring
  3. additionafter the addition the solution
  4. temperaturewas refluxed for 22 hours
  5. customThe solvents were removed
  6. additionH2O was added to the residue
  7. extractionThe solid material was extracted in ethyl acetate
  8. washwashed with H2O
  9. dry with materialdried over MgSO4
  10. customThe MgSO4 was removed by filtration
  11. customthe solvents by evaporation

출처 및 근거

ORD 기록
ord-e0755c513d5243bbab8eaa043e0680ed
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05264437

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