Dichloromethane → HCID 22672630、化合物

HRID 1006676ノート

反応式

HRID 1006676 の反応式
[OH:1][C:2]1[CH:20]=[CH:19][CH:18]=[C:17]([CH3:21])[C:3]=1[CH2:4][NH:5][C:6]1[C:7]2[N:8]([C:12]([CH3:16])=[C:13]([CH3:15])[N:14]=2)[CH:9]=[CH:10][CH:11]=1.[OH-].[K+].[Cl:24][C:25]([O:27][CH3:28])=[O:26].C(Cl)Cl>CC(C)=O>[ClH:24].[C:25](=[O:26])([O:27][CH3:28])[O:1][C:2]1[CH:20]=[CH:19][CH:18]=[C:17]([CH3:21])[C:3]=1[CH2:4][NH:5][C:6]1[C:7]2[N:8]([C:12]([CH3:16])=[C:13]([CH3:15])[N:14]=2)[CH:9]=[CH:10][CH:11]=1

参加物

6

実験手順

A mixture of 8-(2-hydroxy-6-methylbenzylamino)-2,3-dimethylimidazo[1,2-a]pyridine (0.068 g, 0.24 mmol) sodium carbonate (0.12 g, 1.1 mmol), and potassium hydroxide (0.019 g, 0.34 mmol) in acetone (12 ml) was stirred for 15 min in room temperature in a nitrogen atmosphere. Methyl chloroformate (0.023 g, 0.24 mmol) was added and the reaction mixture was stirred for 70 min. Methylene chloride was added and the mixture was filtred and the filtrate was evaporated under reduced pressure. The residue was solved in methylene chloride, washed with saturated sodium bicarbonate and water and the organic layer was separated, dried and evaporated under reduced pressure. The residue was purified by by column chromatography on silica gel using methylene chloride:methanol (100:5) as eluent and treated with HCl/diethyl ether to give 0.025 g (28%) of the title compound.

後処理

  1. stirringthe reaction mixture was stirred for 70 min
  2. customthe filtrate was evaporated under reduced pressure
  3. washwashed with saturated sodium bicarbonate and water
  4. customthe organic layer was separated
  5. customdried
  6. customevaporated under reduced pressure
  7. customThe residue was purified by by column chromatography on silica gel
  8. additiontreated with HCl/diethyl ether

出典と根拠

ORDレコード
ord-a4a5cf6d97b546de9843ee125a49ea3a
出典データセット
uspto-grants-2004_09
特許番号
US06790960B2

反応ノート

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