Potassium Carbonate → HCID 9956212、化合物

HRID 1493499ノート

反応式

HRID 1493499 の反応式
[C:1]([OH:4])(=[O:3])[CH3:2].C[C:6]1[CH:11]=[C:10]([OH:12])[CH:9]=[CH:8][C:7]=1[NH:13][C:14]1[C:19]([Cl:20])=[CH:18][CH:17]=[CH:16][C:15]=1[Cl:21].[C:22](=O)([O-])[O-].[K+].[K+].Cl[CH2:29][C:30]1[CH:39]=[CH:38][C:37]2[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=2)[N:31]=1>C(#N)C.C1OCCOCCOCCOCCOCCOC1>[CH3:22][O:3][C:1](=[O:4])[CH2:2][C:8]1[CH:9]=[C:10]([O:12][CH2:29][C:30]2[CH:39]=[CH:38][C:37]3[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=3)[N:31]=2)[CH:11]=[CH:6][C:7]=1[NH:13][C:14]1[C:15]([Cl:21])=[CH:16][CH:17]=[CH:18][C:19]=1[Cl:20]

参加物

6

実験手順

Under an atmosphere of nitrogen, a mixture of the crude phenol of Step F, above (5.0 g, 15.4 mmol), potassium carbonate (1.3 g, 9.8 mmol), 18-crown-6 (130 mg), and 2-chloromethyl quinoline (4.1 g, 23 mmol) in 50 mL of acetonitrile is stirred at 60° C. for 24 hours (TLC, silica, dichloromethaneMeOH 19:1). The solvent is evaporated and the residue partitioned between ethyl acetate and water (75 mL each). The insolubles are filtered, the layers separated and the organic phase washed with 1N NaOH and brine. After drying (MgSO4) the solvent is removed in vacuo to give 7.0 g of a thick brown oil. The crude product is purified by flash chromatography (silica Merck 60, dichloromethane and dichloromethane-ethyl acetate 19:1) to give the product (4.2 g, clear oil). The oil is triturated with ethanol to give crystalline product (3.98 g, 55.5%, m.p. 90°-91° C., white solid).

後処理

  1. customThe solvent is evaporated
  2. customthe residue partitioned between ethyl acetate and water (75 mL each)
  3. filtrationThe insolubles are filtered
  4. customthe layers separated
  5. washthe organic phase washed with 1N NaOH and brine
  6. dry with materialAfter drying (MgSO4) the solvent
  7. customis removed in vacuo

出典と根拠

ORDレコード
ord-1deed4e3ab034980b46a319222285040
出典データセット
uspto-grants-1991_06
特許番号
US05021576

反応ノート

読み込み中…