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Sodium Iodide → HCID 13338394, compound

HRID 2417676
Notes
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Reaction equation

HRID 2417676 reaction equation
[N:1]1([C:4]2[C:5]3[N:13]([CH2:14][CH3:15])[N:12]=[C:11]([CH3:16])[C:6]=3[N:7]=[C:8]([CH3:10])[N:9]=2)[CH2:3][CH2:2]1.[I-].[Na+]>CC(C)=O>[CH2:14]([N:13]1[C:5]2[C:4]3[N:9]([CH2:2][CH2:3][N:1]=3)[C:8]([CH3:10])=[N:7][C:6]=2[C:11]([CH3:16])=[N:12]1)[CH3:15]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 5238Sodium IodideHCID 133384337-(Aziridin-1-yl)-1-ethyl-3,5-dimethyl-1H-pyrazolo[4,3-d]pyrimidine

Product 1

HCID 13338394HCID 13338394, compoundYield 57%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

The above aziridine (14 g, 0.065 mol) is dissolved in 150 ml acetone and 12 g (0.08 mol) of sodium iodide is added. The mixture is stirred overnight as a solid separates. The cooled mixture is filtered, the filter cake is washed with saturated NaHCO3 solution then water to yield 8 g (57%) of the title compound, mp 168°-170° C.

Workup

  1. filtrationThe cooled mixture is filtered
  2. washthe filter cake is washed with saturated NaHCO3 solution

Sources & evidence

ORD record
ord-c358f2298b774c6ea15b5b92d7b141c3
Source dataset
uspto-grants-1984_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04469868

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes