Potassium Carbonate → 2,6-dichloro-9-cyclohexyl-9H-purine

HRID 452581

反応式

HRID 452581 の反応式
[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([NH:6][CH:7]=[N:8]2)=[C:4]([Cl:11])[N:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH:18]1(I)[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1>CS(C)=O>[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH:18]2[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)=[C:4]([Cl:11])[N:3]=1

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 12289IodocyclohexaneHCID 53244122,6-Dichloropurine

生成物 1

HCID 203416102,6-dichloro-9-cyclohexyl-9H-purine収率 41%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

2,6-Dichloropurine (1 mmol), powdered potasium carbonate (1 mmol) and cyclohexyliodide (4 mmol) were vigorously stirred in 5 mL DMSO overnight. After evaporation of the solvent the product was extracted (water/diethylether) and purified by column chromatography (silicagel/1% MeOH in CHCl3). Crystallization from methanol gave the product in yield 41%, mp 116-121° C.

後処理

  1. customAfter evaporation of the solvent the product
  2. extractionwas extracted (water/diethylether)
  3. custompurified by column chromatography (silicagel/1% MeOH in CHCl3)
  4. customCrystallization from methanol
  5. customgave the product in yield 41%, mp 116-121° C.

出典と根拠

ORDレコード
ord-608eba876df34e16a63e3cf3678de238
出典データセット
uspto-grants-2013_07
特許番号
US08492391B2

関連ノート

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