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Sodium Iodide → HCID 13338380, 화합물

HRID 2417660
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HRID 2417660 반응식
[CH3:1][CH:2]1[CH2:4][N:3]1[C:5]1[C:6]2[N:14]([CH3:15])[N:13]=[C:12]([CH3:16])[C:7]=2[N:8]=[C:9]([CH3:11])[N:10]=1.[I-].[Na+]>CC(C)=O>[CH3:15][N:14]1[C:6]2[C:5]3[N:10]([CH2:4][CH:2]([CH3:1])[N:3]=3)[C:9]([CH3:11])=[N:8][C:7]=2[C:12]([CH3:16])=[N:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5238Sodium IodideHCID 140065651,3,5-Trimethyl-7-(2-methylaziridin-1-yl)-1H-pyrazolo[4,3-d]pyrimidine

생성물 1

HCID 13338380HCID 13338380, 화합물수율 57.5%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

The above aziridine (4.4 g, 0.02 mol) in 50 ml of acetone is stirred under reflux with 3.5 g of sodium iodide for three hours and evaporated in vacuo. The residue is partitioned in 150 ml of methylene dichloride and 50 ml of 20% aqueous sodium carbonate solution. The organic layer is separated, dried (MgSO4) and evaporated in vacuo. The resulting solid is recrystallized from acetonitrile to give 2.5 g of the title compound, mp 169°-172° C.

후처리

  1. customevaporated in vacuo
  2. customThe residue is partitioned in 150 ml of methylene dichloride
  3. customThe organic layer is separated
  4. dry with materialdried (MgSO4)
  5. customevaporated in vacuo
  6. customThe resulting solid is recrystallized from acetonitrile

출처 및 근거

ORD 기록
ord-0dd2833f88254e358151c0255e777577
출처 데이터셋
uspto-grants-1984_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04469868

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