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Ethyl 6-amino-5-methoxyindole-2-carboxylate

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CAS:107575-60-0
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Ethyl 6-amino-5-methoxyindole-2-carboxylate manufacturers

Ethyl 6-amino-5-methoxyindole-2-carboxylate Basic information
Product Name:Ethyl 6-amino-5-methoxyindole-2-carboxylate
Synonyms:ETHYL 6-AMINO-5-METHOXYINDOLE-2-CARBOXYLATE;6-amino-5-methoxyindole-2-carboxylic acid ethyl ester;6-AMino-5-Methoxy indole-2-carboxylate;6-AMino-5-Methoxy-1H-indole-2-carboxylic Acid Ethyl Ester;1H-Indole-2-carboxylic acid, 6-amino-5-methoxy-, ethyl ester;Nicotine Intermediates Ethyl 6-amino-5-methoxyindole-2-carboxylate;methyl 6-amino-5-methoxy-1H-indole-2-carboxylate
CAS:107575-60-0
MF:C12H14N2O3
MW:234.25
EINECS:
Product Categories:Aromatics Compounds;Aromatics;Indole Derivatives;107575-60-0
Mol File:107575-60-0.mol
Ethyl 6-amino-5-methoxyindole-2-carboxylate Structure
Ethyl 6-amino-5-methoxyindole-2-carboxylate Chemical Properties
Melting point 164-166°C
Boiling point 439.3±40.0 °C(Predicted)
density 1.283±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
solubility Soluble in dichloromethane, ethyl acetate and methanol.
pka15.95±0.30(Predicted)
form Solid
color Slightly Yellowish-Brown
Safety Information
Risk Statements 33-36/37/38
Safety Statements 26-37
MSDS Information
ProviderLanguage
ALFA English
Ethyl 6-amino-5-methoxyindole-2-carboxylate Usage And Synthesis
Chemical PropertiesSlightly Yellowish-Brown Solid
UsesEthyl 6-amino-5-methoxyindole-2-carboxylate is a important organic intermediate. It can be used in agrochemical, pharmaceutical and dyestuff field.
Synthesis
ETHYL 6-FORMYLAMINO-5-METHOXYINDOLE-2-CARBOXYLATE

119825-27-3

Ethyl 6-amino-5-methoxyindole-2-carboxylate

107575-60-0

The experimental procedure for the synthesis of ethyl 6-amino-5-methoxyindole-2-carboxylate using pyrroloquinoline impurity 1 as starting material was as follows: the experiment was divided into six groups, each using a different sample solution of heteropolyacid as catalyst. The procedure was as follows: compound 6 (0.524 g, 2 mmol) and benzylamine (0.321 g, 0.328 ml, 3 mmol) were placed in a 10 ml flask, and heteropolyacid ionic liquids (0.04 mmol) were added as catalysts, respectively. The reaction mixture was heated by microwave heating at 140 °C for 90 min. After completion of the reaction, 20 ml of ethyl acetate was added to the mixture and stirred thoroughly for 30 minutes. Subsequently, the mixture was filtered and the filtrate was concentrated to dryness by evaporation and finally purified by recrystallization to obtain the target product compound 7.

References[1] Patent: CN104557921, 2018, B. Location in patent: Paragraph 0101-011
[2] Helvetica Chimica Acta, 1993, vol. 76, # 4, p. 1667 - 1673
[3] Patent: WO2006/102642, 2006, A1. Location in patent: Page/Page column 9; 15; 1/6
[4] Tetrahedron Letters, 1988, vol. 29, # 30, p. 3709 - 3712
Ethyl 6-amino-5-methoxyindole-2-carboxylate Preparation Products And Raw materials
Raw materialsETHYL 6-FORMYLAMINO-5-METHOXYINDOLE-2-CARBOXYLATE
Tag:Ethyl 6-amino-5-methoxyindole-2-carboxylate(107575-60-0) Related Product Information
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