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2-Chloro-10H-pyridazino(6,1-b)quinazolin-10-one → HCID 20284571, 화합물

HRID 127481
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반응식

HRID 127481 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.[CH3:17][O-:18].[Na+]>CO>[CH3:17][O:18][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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 969282-Chloro-10H-pyridazino(6,1-b)quinazolin-10-oneHCID 10942334Sodium Methoxide

생성물 1

HCID 20284571HCID 20284571, 화합물수율 70.9%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

2-Chloro-10H-pyridazino[3,2-b]quinazolin-10-one (2.3 g) and sodium methoxide (1.1 g) in 100 ml of methanol was heated at 60° C. for 5 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 methanol to give 1.6 g of 2-methoxy-10H-pyridazino[3,2-b]-quinazolin-10-one (Compound No. 1). M.P., 222.5°-223.0° 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 methanol

출처 및 근거

ORD 기록
ord-f2a92ad9e11149c287c2f3e9fce12779
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04256483

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