2-Methylimidazole → Ondansetron

HRID 2112265

反応式

HRID 2112265 の反応式
[CH3:1][N:2]1[C:14]2[CH2:13][CH2:12][CH2:11][C:10](=[O:15])[C:9]=2[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2.[CH3:16][C:17]1[NH:18][CH:19]=[CH:20][N:21]=1.N1(CN2CCCCC2)CCCC[CH2:23]1.[Cl-].[Al+3].[Cl-].[Cl-].[OH-].[Na+]>C(#N)C.ClCCl>[CH3:1][N:2]1[C:14]2[CH2:13][CH2:12][CH:11]([CH2:23][N:18]3[CH:19]=[CH:20][N:21]=[C:17]3[CH3:16])[C:10](=[O:15])[C:9]=2[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2

参加物

8

反応物 5

HCID 127492-MethylimidazoleHCID 14798Sodium HydroxideHCID 70151DipiperidinomethaneHCID 5988759-Methyl-1,2,3,9-tetrahydro-4H-carbazol-4-oneHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 4595Ondansetron収率 70%

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 6344Dichloromethane溶媒

実験手順

2.0 g of 1,2,3,9-tetrahydro-9-methyl-4H-carbazol-4-one, 1.65 g of 2-methyl imidazole and 274 g of dipiperidinomethane were suspended in 30 ml of acetonitrile, and then 2 g of aluminum chloride was slowly added thereto. The reaction mixture was stirred under reflux for 10 hours. 150 ml dichloromethane and 50 ml of 1N aq. sodium hydroxide were added to the reaction mixture. The resulting organic layer was separated and dried over MgSO4, and then evaporated. The resulting solid was suspended in acetone and stirred for 3 hours, and then filtered and dried under a reduced pressure to give 2.05 g of title compound (yield 70%).

後処理

  1. temperatureunder reflux for 10 hours
  2. customThe resulting organic layer was separated
  3. dry with materialdried over MgSO4
  4. customevaporated
  5. stirringstirred for 3 hours
  6. filtrationfiltered
  7. customdried under a reduced pressure

出典と根拠

ORDレコード
ord-af9f12dbf1f24e54a0f9c9c78bf2726f
出典データセット
uspto-grants-2009_04
特許番号
US07521565B2

関連ノート

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