Ethyl 5-cyanoindole-2-carboxylate
Ethyl 5-cyanoindole-2-carboxylate Basic information
- Product Name:
- Ethyl 5-cyanoindole-2-carboxylate
- Synonyms:
-
- Ethyl 5-cyanoindole-2-carboxylate
- Methyl 5-cyano-1H-indole-2-carboxylate
- 1H-Indole-2-carboxylic acid, 5-cyano-, ethyl ester
- ETHYL 5-CYANO-1H-INDOLE-2-CARBOXYLATE
- 5-CYANOINDOLE-2-CARBOXYLIC ACID ETHYL ESTER
- 5-CYANO-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER
- 5-cyano-1H-indole-2-carboxylic acid methyl ester
- 2-Hydroxy-4-methyl-6-oxo-1,6-dihydro-3-pyridinecarbonitrile
- CAS:
- 105191-13-7
- MF:
- C12H10N2O2
- MW:
- 214.22
- Mol File:
- 105191-13-7.mol
Ethyl 5-cyanoindole-2-carboxylate Chemical Properties
- Boiling point:
- 419.3±25.0 °C(Predicted)
- Density
- 1.28±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 13.63±0.30(Predicted)
- Appearance
- Off-white to light brown Solid
Ethyl 5-cyanoindole-2-carboxylate Usage And Synthesis
Uses
Ethyl 5-cyanoindole-2-carboxylate is an important chemical raw material for the preparation of pril drugs and dye products, and is also widely used in the pharmaceutical industry.
Synthesis
16732-70-0
544-92-3
105191-13-7
General procedure for the synthesis of ethyl 5-cyano-1H-indole-2-carboxylate: a suspension of cuprous cyanide (27 mg, 0.3 mmol) and ethyl 5-bromoindole-2-carboxylate (138) in 500 μL of DMF was stirred and reacted for 7 hours at 155 °C. After completion of the reaction, it was purified by silica gel column chromatography (3 × 15 cm, SiO?, 20% EtOAc/hexane as eluent) to afford the target product, ethyl 5-cyano-1H-indole-2-carboxylate (139) (34 mg, 63% yield), as a white solid with melting point of 181-182 °C.
References
[1] Patent: US2005/26987, 2005, A1. Location in patent: Page 23
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Ethyl 5-cyanoindole-2-carboxylate(105191-13-7)Related Product Information
- Indole-3-acetic acid
- Ethanol
- Ethyl acetate
- Ethyl N-cyanoethanimideate
- Indole-2-carboxylic acid
- Ethylparaben
- Trinexapac-ethyl
- Tris(trimethylsilyl)phosphate
- Indole-3-butyric acid
- RESMETHRIN
- Ethyl cyanoacetate
- Indole
- ETHYL 2-CYANOACRYLATE
- Ethyl formate
- ISOXADIFEN-ETHYL
- Indometacin
- 2-Ethoxyethanol
- Diethyl ether