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Sodium Bicarbonate → N-(2,2-Diphenylethyl)-2-(methylsulphonyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amine

HRID 10437
ノート
印刷プレビュー

反応式

HRID 10437 の反応式
O[O:2][S:3]([O-:5])=O.[K+].[C:7]1([CH:13]([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[CH2:14][NH:15][C:16]2[N:24]=[C:23](SC)[N:22]=[C:21]3[C:17]=2[N:18]=[CH:19][N:20]3[CH:27]2[CH2:32][CH2:31][CH2:30][CH2:29][O:28]2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[C:39](=O)([O-])O.[Na+]>O.CC(C)=O>[C:33]1([CH:13]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH2:14][NH:15][C:16]2[N:24]=[C:23]([S:3]([CH3:39])(=[O:5])=[O:2])[N:22]=[C:21]3[C:17]=2[N:18]=[CH:19][N:20]3[CH:27]2[CH2:32][CH2:31][CH2:30][CH2:29][O:28]2)[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 516892Sodium BicarbonateHCID 21978277N-(2,2-diphenylethyl)-2-(methylsulphanyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amineHCID 23707502Potassium hydroxy sulfite

生成物 1

HCID 21978255N-(2,2-Diphenylethyl)-2-(methylsulphonyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amine収率 75.7%

試薬・触媒・溶媒 2

HCID 180Acetone
溶媒
HCID 962Water溶媒2 回

実験手順

A solution of Oxone (trade mark) (potassium peroxymonosulphate) (44 g, 71.7 mmol) in water (200 ml) was added dropwise over 2 hours to a solution of N-(2,2-diphenylethyl)-2-(methylsulfanyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine (Preparation 3) (25 g, 56.2 mmol) and sodium hydrogencarbonate (20 g, 238 mmol) in acetone (1000 ml) and water (250 ml). The resultant mixture was stirred at room temperature for 24 hours, filtered and the residue washed with acetone. The acetone was removed from the filtrate under reduced pressure and the resulting aqueous residue extracted with ethyl acetate and then dichloromethane. The combined organic layers were washed with brine, dried with anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure. The residue was triturated with diethyl ether, filtered, washed with diethyl ether and pentane and then dried to afford the title compound as a white solid (20.32 g).

後処理

  1. filtrationfiltered
  2. washthe residue washed with acetone
  3. customThe acetone was removed from the filtrate under reduced pressure
  4. extractionthe resulting aqueous residue extracted with ethyl acetate
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried with anhydrous magnesium sulphate
  7. filtrationfiltered
  8. customthe solvent removed under reduced pressure
  9. customThe residue was triturated with diethyl ether
  10. filtrationfiltered
  11. washwashed with diethyl ether and pentane
  12. customdried

出典と根拠

ORDレコード
ord-c6bbeb5096df4e269e3f46d31c8cd773
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07094769B2

反応ノート

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