2-Thiophenecarboxaldehyde → HCID 54465784、化合物

HRID 1418547ノート

反応式

HRID 1418547 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH:6]=O.[Br:8][C:9]1[C:10]([OH:20])=[C:11]([NH2:19])[C:12](=[C:16]([Br:18])[CH:17]=1)[C:13]([OH:15])=[O:14].[O-]S([O-])(=O)=O.[Na+].[Na+].C([BH3-])#N.[Na+]>CO.C(O)(=O)C>[Br:8][C:9]1[C:10]([OH:20])=[C:11]([NH:19][CH2:6][C:2]2[S:1][CH:5]=[CH:4][CH:3]=2)[C:12](=[C:16]([Br:18])[CH:17]=1)[C:13]([OH:15])=[O:14]

参加物

7

反応物 4

HCID 73642-ThiophenecarboxaldehydeHCID 24436Sodium SulfateHCID 5003444Sodium cyanoborohydrideHCID 99048002-Amino-4,6-dibromo-3-hydroxybenzoic acid

生成物 1

HCID 54465784HCID 54465784、化合物収率 12.3%

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 887Methanol溶媒2 回

実験手順

A solution of 2-thiophenecarboxaldehyde (38 mg, 0.34 mmol) in dry methanol (0.8 mL) was added to a mixture of 4,6-dibromo-3-hydroxyanthranilic acid (105 mg, 0.34 mmol) and Na2SO4 (240 mg, 1.7 mmol) in methanol (2 mL ). The reaction mixture was stirred overnight at room temperature. Sodium cyanoborohydride (32 mg, 0.51 mmol) was added, and the mixture was stirred for 2 days at room temperature. Conc. acetic acid (1 mL) was added, and the solvent was removed in vacuo. The residue was partitioned between brine and EtOAc (20 mL). The layers were separated and the aqueous layer was extracted with EtOAc (20 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure. The obtained material was purified by column chromatography (SiO2, CH2Cl2 -hexane-EtOAc-conc. HOAc 30:30:20:3). Preparative HPLC (H2O-acetonitrile-conc. HOAc 50:50:1) yielded the title compound as a yellowish solid (17 mg): 1H NMR (CD3OD-d4) 7.26 (dd, J=5 Hz, 1 Hz), 7.20 (s 1 H), 6.99 (m, 1 H), 6.92 (dd, J=5 Hz, J=5 Hz, 1 H), 4.54 (s, 2 H); MS (TSP): m/z (rel.int.) 410/408/406 (M+1, 5/12/7), 234/232 (31/28), 154 (100).

後処理

  1. stirringthe mixture was stirred for 2 days at room temperature
  2. customthe solvent was removed in vacuo
  3. customThe residue was partitioned between brine and EtOAc (20 mL)
  4. customThe layers were separated
  5. extractionthe aqueous layer was extracted with EtOAc (20 mL)
  6. dry with materialThe combined organic layers were dried (MgSO4)
  7. concentrationconcentrated under reduced pressure
  8. customThe obtained material was purified by column chromatography (SiO2, CH2Cl2 -hexane-EtOAc-conc. HOAc 30:30:20:3)

出典と根拠

ORDレコード
ord-3ea2c05dfe0246c8947606f9d36ac289
出典データセット
uspto-grants-1999_03
特許番号
US05883129

反応ノート

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