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Dimethylformamide → Diethyl [(6-pivalamido-4-quinazolinylamino)methylene]propanedioate

HRID 2296450
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HRID 2296450 반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]=[CH:9][N:8]=[C:7]2[NH:14][CH:15]=[C:16]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[C:17]([O:19][CH2:20][CH3:21])=[O:18])([O-])=O.CN(C)[CH:29]=[O:30]>[Pd].[H][H]>[C:29]([NH:1][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]=[CH:9][N:8]=[C:7]2[NH:14][CH:15]=[C:16]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[C:17]([O:19][CH2:20][CH3:21])=[O:18])(=[O:30])[C:6]([CH3:11])([CH3:7])[CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6228DimethylformamideHCID 13060485Diethyl[(6-nitro-4-quinazolinylamino)methylene]propanedioate

생성물 1

HCID 13060496Diethyl [(6-pivalamido-4-quinazolinylamino)methylene]propanedioate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 178418361HCID 178418361, 화합물용매2회

실험 절차

A suspension of diethyl [(6-nitro-4-quinazolinylamino)methylene]propanedioate (10.8 g) in N,N-dimethylformamide (380 ml) was shaken with 10% palladium on carbon (3.6 g) in hydrogen atmosphere at ambient temperature until hydrogen gas (2030 ml) was absorbed. The catalyst was removed by filtration and washed with a small volume of N,N-dimethylformamide. To the combined filtrate and washings was added pyridine (17 ml) and the mixture was cooled over an ice-bath. To the solution was added dropwise pivalic chloride (6.33 g) for 20 minutes and then the reaction mixture was stirred for 2 hours and 40 minutes at ambient temperature. To the resultant mixture was added ice-water under stirring and then the mixture was concentrated under reduced pressure. To the residue was added chloroform and then the mixture was washed with an aqueous solution saturated with sodium bicarbonate and with water. Insoluble materials were removed by filtration from the chloroform layer. The filtrate was washed with aqueous solution saturated with sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resultant oil was subjected to a chromatography using silica gel (developing solvent: dichloromethane) to give the first Fraction A and the second Fraction B. The Fraction A was concentrated under reduced pressure to give crystalline diethyl [(6-pivalamido-4-quinazolinylamino)methylene]propanedioate (4.6 g). Further, Fraction B was concentrated under reduced pressure to give a solid (3.6 g), which was suspended in methanol. Insoluble materials were separated by filtration and recrystallized from ethyl acetate to give crystalline diethyl [(6-formamido-4-quinazolinylamino)methylene]propanedioate (0.58 g).

후처리

  1. customwas absorbed
  2. customThe catalyst was removed by filtration
  3. washwashed with a small volume of N,N-dimethylformamide
  4. additionTo the combined filtrate and washings was added pyridine (17 ml)
  5. temperaturethe mixture was cooled over an ice-bath
  6. additionTo the solution was added dropwise pivalic chloride (6.33 g) for 20 minutes
  7. additionTo the resultant mixture was added ice-water
  8. stirringunder stirring
  9. concentrationthe mixture was concentrated under reduced pressure
  10. additionTo the residue was added chloroform
  11. washthe mixture was washed with an aqueous solution saturated with sodium bicarbonate and with water
  12. customInsoluble materials were removed by filtration from the chloroform layer
  13. washThe filtrate was washed with aqueous solution saturated with sodium chloride
  14. dry with materialdried over anhydrous magnesium sulfate
  15. concentrationconcentrated under reduced pressure
  16. customto give the first Fraction A
  17. concentrationThe Fraction A was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7e02ff7252ff4567808e34b7f61b92ca
출처 데이터셋
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04429126

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