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Chemical Structure| 1303426-83-6 Chemical Structure| 1303426-83-6

Structure of 1303426-83-6

Chemical Structure| 1303426-83-6

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Product Details of [ 1303426-83-6 ]

CAS No. :1303426-83-6
Formula : C7H6IN3
M.W : 259.05
SMILES Code : CC1=C2C(NC=C2I)=NC=N1

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Application In Synthesis of [ 1303426-83-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1303426-83-6 ]

[ 1303426-83-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 945950-37-8 ]
  • [ 1303426-83-6 ]
YieldReaction ConditionsOperation in experiment
0.94 g With N-iodo-succinimide; In dichloromethane; at 20℃; for 0.75h; To <strong>[945950-37-8]4-methyl-7H-pyrrolo[2,3-d]pyrimidine</strong> (18, 0.634 g, 4.76 mmol) in 50 mL of dichloromethane, N-iodosuccinimide (1.3 g, 5.7 mmol) was added and the reaction stirred at room temperature for 45 minutes. The reaction was concentrated under vacuum, then ethyl acetate was added and washed with 1 N aqueous sodium thiosulfate. The organic layer was dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography, eluting with 20-100% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound (19, 0.94 g). MS (ESI) [M+H+]+=260.26.
1.69 g With N-iodo-succinimide; In dichloromethane; at 20℃; for 2h; Suspended in 30mL of DCM was 4-methyl -7H- pyrrolo [2,3-d] pyrimidine (1g, 7.51mmol) was added N- iodosuccinimide (1.86g, 8.26mmol).It was stirred at room temperature for 2 hours the reaction mixture.The volatiles were removed in vacuo.Of anhydrous ethyl acetate and 50% saturated NaHCO3The residue obtained was extracted.With water and the organic layer was washed with brine, dried (MgSO4), Filtered and the volatiles removed in vacuo.The residue was suspended in acetonitrile and sonicated for 45 minutes.The solid was collected by filtration to give 5-iodo-4-methyl--7H- pyrrolo [2,3-d] pyrimidine (1.69 g).
  • 2
  • [ 1303426-83-6 ]
  • [ 163226-45-7 ]
  • C35H32IN3O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20℃; for 2h;Inert atmosphere; General procedure: To a mixture of appropriate 3a-e (1.5 mmol), 1 (1.57 mmol) and Ph3P (3.75 mmol) in THF was added DIAD (3.75 mmol) dropwise at 0 C under nitrogen and stirring continued at rt. Completion of reaction was analyzed by TLC, solvent evaporated under reduced pressure and crude was purified by column chromatography on silica gel by eluting up to 30 % ethyl acetate in hexane to give couple products in more than 80 % yield. The deprotection was carried out by heating at 60 C in 10 % HCl in MeOH. After completion (monitored by TLC), the reaction mixture was neutralized by NaHCO3 and purified by silica gel chromatography (10% methanol in DCM) to get 6a-e in 70-85% yield.
 

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