Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate

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Products Intro: Product Name:Ethyl4,5-bis(2-methoxyethoxy)-2-aminobenzoate
CAS:179688-27-8
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Products Intro: Product Name:ethyl 2-amino-4,5-bis(2-methoxyethoxy)benzoate
CAS:179688-27-8
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Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate manufacturers

  • Erlotinib Intermediate
  •  Erlotinib Intermediate pictures
  • $15.00 / 1KG
  • 2020-09-27
  • CAS:179688-27-8
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 500 Ton/Tons per Month
Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate Basic information
Product Name:Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate
Synonyms:Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate;2-Amino-4,5-bis(2-methoxyethoxy)benzoic acid ester;2-Amino-4,5-bis(2-methoxyethoxy)benzoic acid ethyl ester;4,5-Bis(2-methoxyethoxy)anthranilic acid ethyl ester;Methyl 2-amino-4,5-bis(2-methoxyethoxy)benzoate;Ethyl 2-aMino-4,5-bis(2-Methoxyethoxy)benzoate;Erlotinib interMidiate IV;ethyl 2-aMino-4,5-bis(2-Methoxyethoxy)benzoate HCL
CAS:179688-27-8
MF:C15H23NO6
MW:313.35
EINECS:700-551-3
Product Categories:Erlotinib INTERMEDIATES;intermidiate of Erlotinib hydrochloride
Mol File:179688-27-8.mol
Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate Structure
Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate Chemical Properties
Boiling point 456.4±45.0 °C(Predicted)
density 1.148
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka2.52±0.10(Predicted)
Safety Information
MSDS Information
Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate Usage And Synthesis
Uses2-Amino-4,5-bis(2-methoxyethoxy)benzoic Acid Ethyl Ester is an intermediate in the synthesis of Erlotinib (E625000, HCl); a selective epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor and antineoplastic agent.
Synthesis
Ethyl 4,5-bis(2-methoxyethoxy)-2-nitrobenzoate

179688-26-7

Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate

179688-27-8

GENERAL METHOD: A mixture of ethyl 4,5-bis(2-methoxyethoxy)-2-nitrobenzoate (1.0 mmol), hydrazine hydrate (NH2NH2-H2O, 2.5 eq.), and H2O2-treated activated charcoal powder (AC, 50 wt%) in N,N-dimethylformamide (DMF, 1.5 mL) was placed under vigorous magnetic stirring at 100 °C. . The reaction process was monitored by liquid chromatography-mass spectrometry (LC-MS) or gas chromatography-mass spectrometry (GC-MS). Upon completion of the reaction, the reaction mixture was filtered to remove the catalyst. The combined organic phases were dried with anhydrous sodium sulfate (Na2SO4) and filtered. The solvent was removed by distillation under reduced pressure to afford the target product ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate. All the compounds were confirmed by 1H nuclear magnetic resonance (NMR) and mass spectrometry (MS) analysis and validated by comparison with data reported in the literature.

References[1] Journal of Chemical Research, 2017, vol. 41, # 9, p. 509 - 512
[2] Patent: CN107382880, 2017, A. Location in patent: Paragraph 0028
[3] Research on Chemical Intermediates, 2013, vol. 39, # 6, p. 2303 - 2309
[4] Patent: CN103709110, 2016, B. Location in patent: Paragraph 0065; 0066
[5] Journal of Labelled Compounds and Radiopharmaceuticals, 2005, vol. 48, # 11, p. 829 - 843
Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate Preparation Products And Raw materials
Raw materialsEthyl 4,5-bis(2-methoxyethoxy)-2-nitrobenzoate-->Hydrazine hydrate-->N,N-Dimethylformamide
Preparation Products6,7-Bis-(2-methoxyethoxy)-4(3H)-quinazolinone
Tag:Ethyl 4,5-bis(2-methoxyethoxy)-2-aminobenzoate(179688-27-8) Related Product Information
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