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5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE

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Company Name: ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
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Products Intro: Product Name:5,7-Dichloroimidazo[1,2-a]pyrimidine
CAS:57473-32-2
Purity:99% Package:100kg;1.6USD|10kg;6.6USD|1kg;9.6USD
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Products Intro: Product Name:5,7-Dichloroimidazo[1,2-a]pyrimidine
CAS:57473-32-2
Purity:NLT 98% Package:1G;1KG;100KG
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Products Intro: Product Name:5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE
CAS:57473-32-2
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Products Intro: Product Name:5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE
CAS:57473-32-2
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:5,7-Dichloroimidazo[1,2-a]pyrimidine
CAS:57473-32-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-02101

5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE manufacturers

5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE Basic information
Product Name:5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE
Synonyms:5,7-Dichloroimidazo[1,2-a]pyrimidine hydrochloride salt;5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE;5,7-Dichloroimidazo[1,2-α]pyrimidine;Zinc04204219;Imidazo[1,2-a]pyrimidine, 5,7-dichloro-
CAS:57473-32-2
MF:C6H3Cl2N3
MW:188.01
EINECS:
Product Categories:Heterocycle-Pyrimidine series;Heterocyclic Compounds;Bases & Related Reagents;Heterocycles;Nucleotides
Mol File:57473-32-2.mol
5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE Structure
5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE Chemical Properties
Melting point 257-259°C
density 1.69
storage temp. Inert atmosphere,2-8°C
solubility DMSO, Methanol
pka2.31±0.30(Predicted)
form Solid
color Light Yellow
CAS DataBase Reference57473-32-2
Safety Information
MSDS Information
5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE Usage And Synthesis
Chemical PropertiesLight Yellow Solid
Synthesis
5,7-Dihydroxyimidazo[1,2-α]pyrimidine

51647-90-6

5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE

57473-32-2

General procedure for the synthesis of 5,7-dichloroimidazo[1,2-a]pyrimidines from 5,7-dihydroimidazo[1,2-A]pyrimidines: imidazo[1,2-a]pyrimidine-5,7-diol (4 g, 26.49 mmol) was dissolved in phosphorus trichloride (POCl3, 50 mL) and heated to a temperature of 90 °C for 4 hours. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to remove excess POCl3. The residue was quenched with saturated sodium bicarbonate (NaHCO3) solution (100 mL) and subsequently extracted with ethyl acetate (EtOAc, 2 x 60 mL). The organic phases were combined, washed with brine (30 mL), dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to afford the target compound 5,7-dichloroimidazo[1,2-a]pyrimidine (3.5 g, 71% yield) as an off-white solid. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.07 (d, J=1.6Hz, 1H), 7.86 (d, J=1.6Hz, 1H), 7.69 (s, 1H); LCMS (mass spectrometry) analysis showed molecular ion peaks m/z: 187.9 ([M+H]+).

References[1] Patent: WO2018/48930, 2018, A1. Location in patent: Paragraph 00337
[2] Patent: EP1666468, 2006, A1. Location in patent: Page/Page column 64
5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE Preparation Products And Raw materials
Raw materials5,7-Dihydroxyimidazo[1,2-α]pyrimidine-->trichlorophosphate
Tag:5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE(57473-32-2) Related Product Information
5,7-Dihydroxyimidazo[1,2-α]pyrimidine Imidazo[1,2-a]pyrimidine 5,7-DICHLORO-IMIDAZO[1,2-A]PYRIMIDINE

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