ChemicalBook > CAS DataBase List > ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE

ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE

Product Name
ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE
CAS No.
56881-21-1
Chemical Name
ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE
Synonyms
ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE;Ethyl 7-aminothieno[2,3-b]pyrazine-6-carboxylate, 97+%;7-Aminothieno[2,3-b]pyrazine-6-carboxylic acid ethyl ester;Thieno[2,3-b]pyrazine-6-carboxylic acid, 7-amino-, ethyl ester
CBNumber
CB8838715
Molecular Formula
C9H9N3O2S
Formula Weight
223.25
MOL File
56881-21-1.mol
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ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE Property

Melting point:
119.5 °C
Boiling point:
390.4±37.0 °C(Predicted)
Density 
1.429±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
Chloroform (Slightly), Methanol (Slightly, Sonicated)
form 
Solid
pka
0.65±0.40(Predicted)
color 
Pale Yellow to Light Yellow
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Safety

HS Code 
2934999090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
E899665
Product name
Ethyl7-Aminothieno[2,3-b]pyrazine-6-carboxylate
Packaging
1g
Price
$200
Updated
2021/12/16
Apolloscientific
Product number
OR960335
Product name
Ethyl7-aminothieno[2,3-b]pyrazine-6-carboxylate
Packaging
1g
Price
$50
Updated
2021/12/16
AK Scientific
Product number
Y9505
Product name
Ethyl7-aminothieno[2,3-b]pyrazine-6-carboxylate
Packaging
5g
Price
$291
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0141068
Product name
ETHYL-7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE
Purity
95.00%
Packaging
1G
Price
$931.39
Updated
2021/12/16
Chemenu
Product number
CM168078
Product name
Ethyl7-aminothieno[2,3-b]pyrazine-6-carboxylate
Purity
95%+
Packaging
10g
Price
$1067
Updated
2021/12/16
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ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE Chemical Properties,Usage,Production

Synthesis

623-51-8

55557-52-3

56881-21-1

Step 7: Synthesis of ethyl 7-aminothieno[2,3-b]pyrazine-6-carboxylate (7) 3-Chloropyrazine-2-carbonitrile (17.9 g, 128 mmol), sodium carbonate (17.7 g, 167 mmol), and ethyl ethyl-2-mercaptoacetate (18.4 mL, 167 mmol) were dissolved in ethanol (120 mL) and heated and refluxed for 4.5 hours. After completion of the reaction, the reaction was quenched with deionized water (1.5 L) and stirring was continued for 30 minutes. The precipitate was collected by filtration and washed with deionized water. The solid residue was dissolved in ether and filtered to remove the black precipitate. The ether was evaporated under reduced pressure to give pure ethyl 7-aminothieno[2,3-b]pyrazine-6-carboxylate (7) (19.6 g, 68.5% yield). 1H-NMR (400 MHz, CDCl3) δ: 1.42 (t, J=7.2 Hz, 3H), 4.40 (q, J=7.2 Hz, 2H), 6.19 (br s, 1H), 8.58 (d, J=2.2 Hz, 1H), 8.63 (d, J=2.2 Hz, 1H).

References

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 11, p. 3643 - 3647
[2] Tetrahedron, 2008, vol. 64, # 7, p. 1333 - 1344
[3] Patent: WO2011/147764, 2011, A1. Location in patent: Page/Page column 27
[4] Patent: US2013/79341, 2013, A1. Location in patent: Paragraph 0110
[5] Journal of Heterocyclic Chemistry, 1975, vol. 12, p. 513 - 516

ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE Preparation Products And Raw materials

Raw materials

Preparation Products

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ETHYL 7-AMINOTHIENO[2,3-B]PYRAZINE-6-CARBOXYLATE Suppliers

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