Triethylamine → HCID 178515078、化合物

HRID 323616

反応式

HRID 323616 の反応式
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.Cl.[CH2:23]([NH:30][NH2:31])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C(N(CC)CC)C>C(O)C>[CH2:23]([N:30]1[C:15](=[O:17])[C:14]2[C:13](=[O:19])[C:12]3[CH:11]=[CH:10][C:9]([Cl:20])=[CH:8][C:7]=3[NH:6][C:5]=2[C:3]([OH:4])=[N:31]1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

参加物

5

反応物 3

HCID 8471TriethylamineHCID 146540Benzylhydrazine dihydrochlorideHCID 178418477HCID 178418477、化合物

生成物 1

HCID 178515078HCID 178515078、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a stirred suspension of dimethyl-7-chloro-4-hydroxyquinoline-2,3-dicarboxylate (5.00 g, 16.90 mM) and benzylhydrazine dihydrochloride (46.15 g, 236.50 mM) in ethanol (100 mL) was added triethylamine (75.8 mL, 541.0 mM). The mixture was heated to give a brown solution which was refluxed for 40 hours during which time a precipitate formed. The suspension was cooled to room temperature and filtered to give the benzylhydrazine salt of the title compound as an impure yellow solid. Multiple crystallizations from ethanolic hydrogen chloride and methanol gave the title compound (0.370 g, 6%) as a white powder, mp 347-350° C.; MS(CI): 354 (M+H).

後処理

  1. temperatureThe mixture was heated
  2. customto give a brown solution which
  3. temperaturewas refluxed for 40 hours during which time a precipitate
  4. customformed
  5. filtrationfiltered

出典と根拠

ORDレコード
ord-f8c16bbecf424a2f81a68afe47b94588
出典データセット
uspto-grants-2001_04
特許番号
US06214826B1

関連ノート

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