Water → 7-Chloro-1-hydroxy-3-(4-chlorophenyl)-3,4,5,10-tetrahydropyridazino[4,5-b]quinoline-4,10-dione

HRID 323620

반응식

HRID 323620 반응식
CO[C:3]([C:5]1[C:14]([C:15]([O:17]C)=O)=[C:13]([OH:19])[C:12]2[C:7](=[CH:8][C:9]([Cl:20])=[CH:10][CH:11]=2)[N:6]=1)=[O:4].[Cl:21][C:22]1[CH:27]=[CH:26][C:25]([NH:28][NH2:29])=[CH:24][CH:23]=1.C(N(CC)CC)C.O>C(O)C>[Cl:20][C:9]1[CH:10]=[CH:11][C:12]2[C:13](=[O:19])[C:14]3[C:15]([OH:17])=[N:29][N:28]([C:25]4[CH:26]=[CH:27][C:22]([Cl:21])=[CH:23][CH:24]=4)[C:3](=[O:4])[C:5]=3[NH:6][C:7]=2[CH:8]=1

참가 물질

6

실험 절차

To a stirred suspension of dimethyl-7-chloro-4-hydroxyquinoline-2,3-dicarboxylate (2.50 g, 8.45 mM) and 4-chlorophenylhydrazine (10.60 g, 59.20 mM) in ethanol (50 mL) was added triethylamine (9.43 mL) to give a brown solution. This solution was refluxed for 24 hours and then cooled to room temperature. Dilution with water (25 mL) gave a brown precipitate. This suspension was stirred for 16 hours and filtered to remove the solids which were discarded. The filtrate formed another precipitate after standing for seven days. This solid was collected and washed with aqueous methanol (50%) and ether to give the 4-chlorophenylhydrazine salt of the title compound as a brown powder (1.20 g). This material was refluxed in glacial acetic acid (25 mL) for 3 hours and cooled to room temperature. The resulting orange suspension was filtered, and the solids were washed with glacial acetic acid and ether to give the title compound (0.810 g, 25%) as a light orange powder, mp 399-401° C.; MS(CI): 374 (M+H).

후처리

  1. customto give a brown solution
  2. temperatureThis solution was refluxed for 24 hours
  3. filtrationfiltered
  4. customto remove the solids which
  5. customThe filtrate formed another precipitate
  6. waitafter standing for seven days
  7. customThis solid was collected
  8. washwashed with aqueous methanol (50%) and ether

출처 및 근거

ORD 기록
ord-ccc049cf5a694efd8cba87cf9eeaff82
출처 데이터셋
uspto-grants-2001_04
특허 번호
US06214826B1

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