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2-Amino-5-chlorobenzoic acid → 8-Chloro-10-oxo-10H-pyridazino[6,1-b]quinazoline-2-carboxylic acid

HRID 1413422
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반응식

HRID 1413422 반응식
[Cl:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=O)[C:5]([NH2:11])=[CH:4][CH:3]=1.Cl[C:13]1[N:18]=[N:17][C:16]([C:19]([OH:21])=[O:20])=[CH:15][CH:14]=1>C(O)(=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]=[C:13]3[CH:14]=[CH:15][C:16]([C:19]([OH:21])=[O:20])=[N:17][N:18]3[C:7](=[O:9])[C:6]=2[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 124762-Amino-5-chlorobenzoic acidHCID 64157626-chloropyridazine-3-carboxylic Acid

생성물 1

HCID 126656848-Chloro-10-oxo-10H-pyridazino[6,1-b]quinazoline-2-carboxylic acid수율 54.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 5-chloroanthranilic acid (5.4 g, 31.6 mmol) and 6-chloropyridazine-3-carboxylic acid (5.0 g, 31.6 mmol) is heated at reflux in acetic acid (50 ml) for 80 hrs. The mixture is cooled and the precipitate which formes is collected to give 4.73 g of crude product, m.p. 253°-300° C. (dec.). Recrystallization of this material from pyridine gives the analytical material, m.p. 260°-262° C.

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후처리

  1. temperatureis heated
  2. temperatureThe mixture is cooled
  3. customthe precipitate which formes is collected

출처 및 근거

ORD 기록
ord-82580a6fdd044ba4a9c07381fd01330b
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04250177

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