4-CHLOROTHIENO[2,3-B]PYRIDINE-5-CARBONITRILE
- Product Name
- 4-CHLOROTHIENO[2,3-B]PYRIDINE-5-CARBONITRILE
- CAS No.
- 63873-61-0
- Chemical Name
- 4-CHLOROTHIENO[2,3-B]PYRIDINE-5-CARBONITRILE
- Synonyms
- 6-bromo-5-fluoro-1,3-dihydroindol-4-one;4-CHLOROTHIENO[2,3-B]PYRIDINE-5-CARBONITRILE;Thieno[2,3-b]pyridine-5-carbonitrile, 4-chloro-
- CBNumber
- CB9848614
- Molecular Formula
- C8H3ClN2S
- Formula Weight
- 194.64
- MOL File
- 63873-61-0.mol
4-CHLOROTHIENO[2,3-B]PYRIDINE-5-CARBONITRILE Property
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- Appearance
- Yellow to brown Solid
Safety
- HS Code
- 2934999090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- C411528
- Product name
- 4-Chlorothieno[2,3-b]pyridine-5-carbonitrile
- Packaging
- 100mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- OR913377
- Product name
- 4-Chlorothieno[2,3-b]pyridine-5-carbonitrile
- Purity
- 95%
- Packaging
- 250mg
- Price
- $250
- Updated
- 2021/12/16
- Product number
- 7H37-5-03
- Product name
- 4-Chlorothieno[2,3-b]pyridine-5-carbonitrile
- Purity
- 95%
- Packaging
- 250mg
- Price
- $400
- Updated
- 2021/12/16
- Product number
- OR913377
- Product name
- 4-Chlorothieno[2,3-b]pyridine-5-carbonitrile
- Purity
- 95%
- Packaging
- 1g
- Price
- $595
- Updated
- 2021/12/16
- Product number
- 7H37-5-03
- Product name
- 4-Chlorothieno[2,3-b]pyridine-5-carbonitrile
- Purity
- 95%
- Packaging
- 1g
- Price
- $952
- Updated
- 2021/12/16
4-CHLOROTHIENO[2,3-B]PYRIDINE-5-CARBONITRILE Chemical Properties,Usage,Production
Synthesis
63873-60-9
63873-61-0
The general procedure for the synthesis of 4-chlorothieno[2,3-b]pyridine-5-carbonitrile as starting material via chlorination was as follows: first, bis-(2-thienylammonium) hexachlorostannate (2) was produced by the reduction of 2-nitrothiophene (1) by the reaction of tin and hydrochloric acid. Subsequently, the compound was subjected to a condensation reaction with ethyl (ethoxymethylene) cyanoacetate in pyridine at 40-50 °C over 24 h to give ethyl α-cyano-β-(N-2-thienylammonium) acrylate (3) in 88% yield. Next, 4-hydroxythieno[2,3-b]pyridine-5-carbonitrile (4) was isolated in 78% yield by refluxing the acrylate through Dowtherm at 250 °C for 40 min, which induced cyclization of the acrylate, followed by precipitation from petroleum ether. Finally, compound 4 was refluxed with phosphoryl chloride at 110 °C for 6 h for chlorination reaction to afford the target product 4-chlorothieno[2,3-b]pyridine-5-carbonitrile (5) in 76% yield.
References
[1] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 17, p. 8196 - 8204
[2] Synthetic Communications, 2013, vol. 43, # 24, p. 3373 - 3386
[3] Heterocycles, 1977, vol. 6, p. 727 - 729
[4] Journal of Heterocyclic Chemistry, 1977, vol. 14, p. 807 - 812
4-CHLOROTHIENO[2,3-B]PYRIDINE-5-CARBONITRILE Preparation Products And Raw materials
Raw materials
Preparation Products
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