5-chloropyrazine-2-carboxamide

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Products Intro: Product Name:5-Chloropyrazine-2-carboxamide
CAS:21279-64-1
Purity:98% Min. Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:21279-64-1
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CAS:21279-64-1
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CAS:21279-64-1
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Products Intro: Product Name:5-chloropyrazine-2-carboxamide
CAS:21279-64-1
Purity:0.97 Package:1KG;25KG

5-chloropyrazine-2-carboxamide manufacturers

5-chloropyrazine-2-carboxamide Basic information
Product Name:5-chloropyrazine-2-carboxamide
Synonyms:5-chloropyrazine-2-carboxamide;5-Chloro-2-pyrazinecarboxamide;EOS-61239;2-Pyrazinecarboxamide, 5-chloro-
CAS:21279-64-1
MF:C5H4ClN3O
MW:157.56
EINECS:1312995-182-4
Product Categories:
Mol File:21279-64-1.mol
5-chloropyrazine-2-carboxamide Structure
5-chloropyrazine-2-carboxamide Chemical Properties
Melting point 171-172 °C
Boiling point 331.3±42.0 °C(Predicted)
density 1.478±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka13.62±0.50(Predicted)
AppearanceOff-white to yellow Powder
Safety Information
MSDS Information
5-chloropyrazine-2-carboxamide Usage And Synthesis
Synthesis
Methyl 5-chloropyrazine-2-carboxylate

33332-25-1

5-chloropyrazine-2-carboxamide

21279-64-1

General procedure for the synthesis of 5-chloropyrazine-2-carboxamide from methyl 5-chloropyrazine-2-carboxylate: Step 1: Ammonium chloride (558 mg, 10.4 mmol) was suspended in benzene (5 mL), and a toluene solution of 2M trimethylaluminum (5.2 mL, 10.4 mmol) was added slowly and dropwise at 0 °C. After stirring for 1 h, a solution of methyl 5-chloropyrazine-2-carboxylate (600 mg, 3.48 mmol) in benzene (5 mL) was added. The reaction mixture was heated to 50 °C and stirred overnight. After the reaction was completed and cooled to room temperature, the reaction mixture was poured into water and neutralized with saturated aqueous sodium bicarbonate. The mixture was extracted with ethyl acetate and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: dichloromethane/methanol = 100:0 → 98:2) to afford 5-chloropyrazine-2-carboxamide (236 mg, 43% yield) as a white solid.

References[1] Patent: WO2009/145360, 2009, A1. Location in patent: Page/Page column 71
[2] Patent: EP2123651, 2009, A1. Location in patent: Page/Page column 21
5-chloropyrazine-2-carboxamide Preparation Products And Raw materials
Raw materialsMethyl 5-chloropyrazine-2-carboxylate-->Toluene-->Benzene-->Trimethylaluminium-->Ammonium chloride
Tag:5-chloropyrazine-2-carboxamide(21279-64-1) Related Product Information
5-CHLOROPYRIDINE-2-BORONIC ACID PINACOL ESTER 5-Chloropyrazolo[1,5-a]pyrimidine ETHYL 5-CHLOROPYRIDINE-2-CARBOXYLATE diMethyl 5-chloropyridine-2,3-dicarboxylate Cefepime 5-Chloropyridine-2-carboxamide 5-CHLORO-2-FORMYLPYRIDINE 5-Chloropyrazolo[1,5-a]pyriMidine-3-carbonitrile 3-CHLORO-5-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)PYRIDINE 5-CHLOROPYRIDO[4,3-B]PYRAZINE 5-CHLORO-PYRIDINE-3-CARBALDEHYDE Pyrazinecarboxylic acid, 5-chloro-, ethyl ester Sulfachoropyrazine sodium

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