Basic information Uses Safety Supplier Related

2-BROMO-6-ETHOXYCARBONYLBENZOTHIAZOLE

Basic information Uses Safety Supplier Related

2-BROMO-6-ETHOXYCARBONYLBENZOTHIAZOLE Basic information

Product Name:
2-BROMO-6-ETHOXYCARBONYLBENZOTHIAZOLE
Synonyms:
  • 2-BROMO-6-ETHOXYCARBONYLBENZOTHIAZOLE
  • Ethyl 2-bromo-6-benzothiazolecarboxylate
  • 6-Benzothiazolecarboxylic acid, 2-bromo-, ethyl ester
  • 2-BROMOBENZOTHIAZOLE-6-CARBOXYLIC ACID
  • Ethyl 2-bromobenzothiazole-6-carboxylate
  • JR-14054, Ethyl 2-bromobenzo[d]thiazole-6-carboxylate, 95%
  • ethyl 2-bromobenzo[d]thiazole-6-carboxylate
  • ethyl 2-broMo-1,3-benzothiazole-6-carboxylate
CAS:
99073-88-8
MF:
C10H8BrNO2S
MW:
286.14
Mol File:
99073-88-8.mol
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2-BROMO-6-ETHOXYCARBONYLBENZOTHIAZOLE Chemical Properties

Boiling point:
377.6±34.0 °C(Predicted)
Density 
1.618±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-1.37±0.10(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

RIDADR 
UN2811
HS Code 
2934208090
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2-BROMO-6-ETHOXYCARBONYLBENZOTHIAZOLE Usage And Synthesis

Uses

2-Bromobenzothiazole-6-carboxylic acid ethyl ester can be used as a pharmaceutical synthesis intermediate.

Synthesis

50850-93-6

99073-88-8

General procedure for the synthesis of ethyl 2-bromobenzothiazole-6-carboxylate from ethyl 2-aminobenzothiazole-6-carboxylate: commercially available ethyl 2-aminobenzothiazole-6-carboxylate (10 g, 45 mmol) was dissolved in acetonitrile (40 mL), and this solution was then added to a solution containing copper(II) bromide (12 g, 54 mmol) and tert-butyl nitrite (9 mL, 75 mmol) in a solution of acetonitrile (100 mL). The reaction was carried out at room temperature and under nitrogen protection with continuous stirring for 45 min. Upon completion of the reaction, the reaction mixture was diluted with 1N HCl (300 mL) and subsequently extracted with dichloromethane (3 x 300 mL). The organic extracts were combined, washed with water (300 mL), dried with anhydrous magnesium sulfate, filtered through a silica gel plug, and finally the solvent was removed under reduced pressure to afford the target product ethyl 2-bromobenzothiazole-6-carboxylate (Step 1) as an off-white solid (11.5 g, 89% yield). The product was characterized by 1H NMR (CDCl3): δ 1.40 (t, 3H), 4.40 (q, 2H), 8.00 (d, 1H), 8.20 (d, 1H), 8.60 (s, 1H).

References

[1] Patent: EP2766359, 2016, B1. Location in patent: Paragraph 0319
[2] Patent: WO2004/63155, 2004, A1. Location in patent: Page 148-149
[3] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 6, p. 1874 - 1879
[4] Yakugaku Zasshi, 1958, vol. 78, p. 437
[5] Chem.Abstr., 1958, p. 14589

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