5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine

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Products Intro: Product Name:5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine
CAS:862729-13-3
Purity:98% Package:5KG;1KG
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Products Intro: Product Name:5-Iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine
CAS:862729-13-3
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-30780
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CAS:862729-13-3
Package:100g,1kg
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Products Intro: Product Name:5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine
CAS:862729-13-3
Purity:0.97 Package:1KG;25KG
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Products Intro: Product Name:5-iodo-7-methylpyrrolo[2,3-d]pyrimidin-4-amine
CAS:862729-13-3
Purity:0.98 Package:1g; 5g; 10g; 25g; 100g
5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine Basic information
Product Name:5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine
Synonyms:5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine;7H-Pyrrolo[2,3-d]pyriMidin-4-aMine, 5-iodo-7-Methyl-;5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine;5-iodo-7-methylpyrrolo[2,3-d]pyrimidin-4-amine;4-Amino-5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidine
CAS:862729-13-3
MF:C7H7IN4
MW:274.06
EINECS:
Product Categories:
Mol File:862729-13-3.mol
5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine Structure
5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine Chemical Properties
Boiling point 436.3±40.0 °C(Predicted)
density 2.24±0.1 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
pka5.07±0.30(Predicted)
AppearanceLight brown to gray Solid
InChIInChI=1S/C7H7IN4/c1-12-2-4(8)5-6(9)10-3-11-7(5)12/h2-3H,1H3,(H2,9,10,11)
InChIKeyVNFSLRASQZPDFQ-UHFFFAOYSA-N
SMILESC1=NC(N)=C2C(I)=CN(C)C2=N1
Safety Information
MSDS Information
5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine Usage And Synthesis
Synthesis
4-AMino-5-iodopyrrolo[2,3-d]pyriMidine

163622-50-2

Iodomethane

74-88-4

5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine

862729-13-3

GENERAL STEPS: To a solution of 750 mg (2.88 mmol) of 5-iodo-7H-pyrrolo[2,3-d]pyrimidin-4-amine dissolved in 20 mL of anhydrous N,N-dimethylformamide (DMF), 190 μL (3.02 mmol) of iodomethane and 795 mg (5.76 mmol) of anhydrous potassium carbonate were added. The reaction mixture was stirred for 8 h at room temperature. After completion of the reaction, the solvent was removed by rotary evaporator. The residue was dissolved in dichloromethane (DCM) and washed with deionized water. The organic layer was dried with anhydrous sodium sulfate, filtered and the solvent was again removed by rotary evaporator to give 394 mg (50% yield) of the target compound 5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine. High resolution mass spectrometry (HRMS, electrospray ionization ESI) analysis resulted in the calculated value of C7H7N4I [M + H]+ 274.9788 and the measured value of 274.9788, which is in agreement with expectations.

References[1] Patent: WO2014/184069, 2014, A1. Location in patent: Page/Page column 34; 35
Tag:5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine(862729-13-3) Related Product Information
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