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ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate

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Products Intro: Product Name:Ethyl 5-amino-2,6-dichloropyrimidine-4-carboxylate
CAS:54368-62-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-26324
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Products Intro: Product Name:ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate
CAS:54368-62-6
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Products Intro: Product Name:5-Amino-2,6-dichloro-4-pyrimidinecarboxylic acid ethyl ester
CAS:54368-62-6
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Products Intro: Product Name:Ethyl 5-amino-2,6-dichloropyrimidine-4-carboxylate
CAS:54368-62-6
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Products Intro: Product Name:ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate
CAS:54368-62-6
Package:5g;100g;1KG;25KG

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ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate Basic information
Product Name:ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate
Synonyms:ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate;5-AMino-2,6-dichloro-pyriMidine-4-carboxylic acid ethyl ester;5-Amino-2,6-dichloro-4-pyrimidinecarboxylic acid ethyl ester;4-Pyrimidinecarboxylic acid, 5-amino-2,6-dichloro-, ethyl ester
CAS:54368-62-6
MF:C7H7Cl2N3O2
MW:236.06
EINECS:
Product Categories:
Mol File:54368-62-6.mol
ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate Structure
ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate Chemical Properties
Boiling point 358.0±37.0 °C(Predicted)
density 1.508±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka-4.07±0.10(Predicted)
AppearanceLight yellow to yellow Solid
InChIInChI=1S/C7H7Cl2N3O2/c1-2-14-6(13)4-3(10)5(8)12-7(9)11-4/h2,10H2,1H3
InChIKeyCAUKXOUUXPKJQC-UHFFFAOYSA-N
SMILESC1(Cl)=NC(Cl)=C(N)C(C(OCC)=O)=N1
Safety Information
MSDS Information
ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate Usage And Synthesis
Synthesis
ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE

54368-61-5

ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate

54368-62-6

Ethyl 2,6-dichloro-5-nitropyrimidine-4-carboxylate (1 g, 3.76 mmol, 1.00 eq.) was used as starting material to form a suspension with stannous chloride dihydrate (3.38 g, 14.98 mmol, 1.00 eq.) in ethyl acetate (30 mL). The mixture was transferred to a 50 mL sealed tube and the reaction was stirred at 70 °C for 5 hours. Upon completion of the reaction, the resulting solution was diluted with 50 mL of water and the pH was adjusted with sodium carbonate to 9. Subsequently, extraction was carried out with ethyl acetate (3 x 100 mL), and the organic phases were combined, washed sequentially with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the resulting residue was purified by silica gel column chromatography with the eluent ethyl acetate/petroleum ether (1:5) to afford the target product ethyl 5-amino-2,6-dichloro-4-pyrimidinecarboxylate (572 mg, 64% yield) as a light yellow solid.LC-MS (ES, m/z): 236 [M + H]+.

References[1] Patent: US2015/57260, 2015, A1. Location in patent: Paragraph 0743; 0744; 1003; 1004
[2] Patent: WO2015/25026, 2015, A1. Location in patent: Page/Page column 174
ethyl 5-aMino-2,6-dichloropyriMidine-4-carboxylate Preparation Products And Raw materials
Raw materialsETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE-->Ethyl acetate
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