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Iodoacetamide → HCID 69930291、化合物

HRID 532524
ノート
印刷プレビュー

反応式

HRID 532524 の反応式
[N:1]1[NH:2][CH:3]=[C:4]2[CH2:8][N:7]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:6][C:5]=12.[H-].[Na+].I[CH2:19][C:20]([NH2:22])=[O:21]>C(#N)C>[NH2:22][C:20](=[O:21])[CH2:19][N:2]1[CH:3]=[C:4]2[CH2:8][N:7]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:6][C:5]2=[N:1]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3727IodoacetamideHCID 24758Sodium hydrideHCID 178451520HCID 178451520、化合物

生成物 1

HCID 69930291HCID 69930291、化合物

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

A 2 L three neck flask fitted with a thermometer, a mechanical stirrer and an addition funnel was charged with a suspension of tert-butyl 2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate (18.01 g, 86.5 mmol) in anhydrous acetonitrile (1.0 L). Sodium hydride (60% dispersion in oil, 4.15 g, 104 mmol) was added to the suspension in one portion under nitrogen. The reaction was stirred at room temperature for 2 h. The resulting white suspension was then cooled in an ice bath and iodoacetamide (31.95 g, 173 mmol) was added. The ice bath was then removed and the mixture was stirred 18 h at room temperature. The mixture was quenched with water (50 mL) and the solvent was removed under reduced pressure. The residue was partitioned between diluted NaCl (50 mL brine and 100 mL water) and 1.0 L EtOAc. The aqueous layer was extracted with 2×1.0 L EtOAc. The organic layers were combined and dried over Na2SO4 and solvent was evaporated under reduced pressure. Crude material was purified on silica gel eluting with 20-50% EtOAc/CH2Cl2 to wash out excess iodoacetamide, and then with 2-10% MeOH/CH2Cl2 to afford a mixture of the two products which were separated on a chiral AD column by eluting with 30% MeOH/CO2 to afford the title compound (less mobile fraction). LC-MS=267.32 [M+1].

後処理

  1. temperatureThe resulting white suspension was then cooled in an ice bath
  2. customThe ice bath was then removed
  3. stirringthe mixture was stirred 18 h at room temperature
  4. customThe mixture was quenched with water (50 mL)
  5. customthe solvent was removed under reduced pressure
  6. customThe residue was partitioned between diluted NaCl (50 mL brine and 100 mL water) and 1.0 L EtOAc
  7. extractionThe aqueous layer was extracted with 2×1.0 L EtOAc
  8. dry with materialdried over Na2SO4 and solvent
  9. customwas evaporated under reduced pressure
  10. customCrude material was purified on silica gel eluting with 20-50% EtOAc/CH2Cl2
  11. washto wash out excess iodoacetamide
  12. customwith 2-10% MeOH/CH2Cl2 to afford
  13. additiona mixture of the two products which
  14. customwere separated on a chiral AD column
  15. washby eluting with 30% MeOH/CO2

出典と根拠

ORDレコード
ord-bc32cfc39c0f485eac349bffdf59ef31
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08853212B2

反応ノート

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