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Ethanol → HCID 20284570, 화합물

HRID 127480
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HRID 127480 반응식
Cl[C:2]1[CH:3]=[CH:4][C:5]2[N:14]([N:15]=1)[C:13](=[O:16])[C:12]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N:6]=2.[OH-].[Na+].[CH2:19]([OH:21])[CH3:20]>O>[CH2:19]([O:21][C:2]1[CH:3]=[CH:4][C:5]2[N:14]([N:15]=1)[C:13](=[O:16])[C:12]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N:6]=2)[CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 969282-Chloro-10H-pyridazino(6,1-b)quinazolin-10-one

생성물 1

HCID 20284570HCID 20284570, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To 1.2 g of 2-chloro-10H-pyridazino[3,2-b]quinazolin-10-one dissolved in ethanol, there was added a solution of sodium hydroxide (2.0 g) in water (8 ml), and stirring was continued at 40° C. for 2 hours. After completion of the reaction, the solvent was removed by distillation, followed by addition of an aqueous solution of acetic acid. The precipitates were collected by filtration and recrystallized from a mixture of methanol and water to give 1.0 g of 2-ethoxy-10H-pyridazino[3,2-b]quinazolin-10-one (Compound No. 2). M.P., 159.5°-160.5° C.

후처리

  1. customAfter completion of the reaction
  2. customthe solvent was removed by distillation
  3. additionfollowed by addition of an aqueous solution of acetic acid
  4. filtrationThe precipitates were collected by filtration
  5. customrecrystallized from a mixture of methanol and water

출처 및 근거

ORD 기록
ord-6a23e1ee58b640d7aa9aabc5074cf1cc
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04256483

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