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7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:7-Chloropyrazolo[1,5-a]pyrimidine
CAS:58347-49-2
Purity:97%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:7-chloropyrazolo[1,5-a]pyrimidine
CAS:58347-49-2
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE
CAS:58347-49-2
Purity:95% Package:1KG;1USD
Company Name: Accela ChemBio Inc.
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Products Intro: Product Name:7-Chloropyrazolo[1,5-a]pyrimidine
CAS:58347-49-2
Purity:>=95% Package:0.1g;0.25g;1g;5g;10g;25g;100g
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:7-Chloropyrazolo[1,5-a]pyrimidine
CAS:58347-49-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-12520

7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE manufacturers

7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE Basic information
Uses
Product Name:7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE
Synonyms:7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE;Pyrazolo[1,5-a]pyrimidine, 7-chloro-
CAS:58347-49-2
MF:C6H4ClN3
MW:153.57
EINECS:
Product Categories:Heterocycle-Pyrimidine series
Mol File:58347-49-2.mol
7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE Structure
7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE Chemical Properties
Melting point 96-98℃
density 1.51
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form Powder
pka-0.59±0.40(Predicted)
color Off-white to yellow to pink to brown
InChIInChI=1S/C6H4ClN3/c7-5-1-3-8-6-2-4-9-10(5)6/h1-4H
InChIKeyYCZQHXPIKQHABJ-UHFFFAOYSA-N
SMILESC12=CC=NN1C(Cl)=CC=N2
Safety Information
HS Code 2933998090
MSDS Information
7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE Usage And Synthesis
Uses7-Clopizo[1,5-A]pyrimidine is a heterocyclic organic compound that can be used as an organic intermediate.
Synthesis
4H-PYRAZOLO[1,5-A]PYRIMIDIN-7-ONE

29274-23-5

7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE

58347-49-2

Pyrazolo[1,5-a]pyrimidin-7(4H)-one (0.50 g, 3.70 mmol) was added with phosphorus trichloride (0.88 mL, 9.62 mmol) and diisopropylethylamine (DIEA, 0.13 mL, 0.74 mmol), mixed well and then the reaction was stirred at 90 °C overnight. After completion of the reaction, the reaction mixture was slowly poured into ice water and extracted with dichloromethane, and the extract was washed with brine. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate = 9:1) to afford the target compound 7-chloropyrazolo[1,5-a]pyrimidine (83 mg, 71% yield).LRMS (m/z): 154 (M + 1)+.1H NMR (400 MHz, DMSO-d6) δ ppm: 6.93 (d, 1H), 7.43 (d, 1H), 8.37 (d, 1H), 8.37 (d, 1H). 1H), 8.37 (d, 1H), 8.52 (d, 1H).

References[1] Patent: EP2518071, 2012, A1. Location in patent: Page/Page column 38
[2] Patent: WO2012/146667, 2012, A1. Location in patent: Page/Page column 90
[3] Patent: WO2012/146666, 2012, A1. Location in patent: Page/Page column 160
[4] Patent: WO2007/17678, 2007, A1. Location in patent: Page/Page column 44
[5] Journal of Medicinal Chemistry, 1981, vol. 24, # 5, p. 610 - 613
7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE Preparation Products And Raw materials
Raw materials4H-PYRAZOLO[1,5-A]PYRIMIDIN-7-ONE
Tag:7-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE(58347-49-2) Related Product Information
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