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N,N-Dimethylaniline → 7-Hydroxy-4-ethoxyquinazoline

HRID 468555
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HRID 468555 반응식
[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:12])[NH:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1.P(Cl)(Cl)(Cl)=O.CN(C)[C:20]1C=CC=C[CH:21]=1.[Na]>C(O)C>[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([O:12][CH2:20][CH3:21])=[N:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 949N,N-DimethylanilineHCID 24813Phosphorus oxychlorideHCID 5360545SodiumHCID 135451644Quinazoline-4,7-diol

생성물 1

HCID 1358487477-Hydroxy-4-ethoxyquinazoline

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

A mixture of 7-hydroxyquinazolin-4-one (105 mg, 648 μmol), phosphorous oxychloride (2 ml), and dimethylaniline (85 μl, 671 μmol) was heated at reflux for 15 minutes in an argon atmosphere. The cooled mixture was concentrated under vacuum, and kept in an argon atmosphere to avoid hydrolysis. This residue was dissolved in ethanol (anhydrous, 3 mL), and a solution of sodium (283 mg, 12.34 mmol) in ethanol (3 ml) was added dropwise. The resulting yellow mixture was stirred at room temperature under argon for 2 hours, acidified to pH 6 using NaH2PO4 and extracted with ethyl acetate (3×50 mL). The combined extracts were dried (MgSO4), filtered and concentrated. The white solid (156 mg) was used without further purification.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 15 minutes in an argon atmosphere
  3. concentrationThe cooled mixture was concentrated under vacuum
  4. customhydrolysis
  5. extractionextracted with ethyl acetate (3×50 mL)
  6. dry with materialThe combined extracts were dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe white solid (156 mg) was used without further purification

출처 및 근거

ORD 기록
ord-087d493118684249a952701671a8ab1f
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08624025B2

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