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Water → Quinazoline, 2-chloro-4,6-dimethoxy-

HRID 1666654
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HRID 1666654 반응식
[Cl:1][C:2]1[N:11]=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:13][CH3:14])[CH:8]=2)[N:3]=1.[CH3:15][O-:16].[Na+].O>CO>[Cl:1][C:2]1[N:11]=[C:10]([O:16][CH3:15])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:13][CH3:14])[CH:8]=2)[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 99913972,4-Dichloro-6-methoxyquinazolineHCID 10942334Sodium Methoxide

생성물 1

HCID 57970127Quinazoline, 2-chloro-4,6-dimethoxy-수율 61.8%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 2,4-dichloro-6-methoxyquinazoline (0.33 g) in methanol (5 mL) was added sodium methoxide (0.086 g), and the mixture was stirred at room temperature for 6 h. Water was added to the reaction mixture, and the aqueous layer was extracted with chloroform. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (silica gel, chloroform/methanol=50:1) to obtain 2-chloro-4,6-dimethoxyquinazoline (0.20 g).

후처리

  1. extractionthe aqueous layer was extracted with chloroform
  2. concentrationThe organic layer was concentrated under reduced pressure
  3. customthe residue was purified by silica gel column chromatography (silica gel, chloroform/methanol=50:1)

출처 및 근거

ORD 기록
ord-6d727b1e7438465ca9d6a98437927d71
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044068B2

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