2-BROMO-4-CHLOROTHIENO[3,2-C]PYRIDINE
2-BROMO-4-CHLOROTHIENO[3,2-C]PYRIDINE Basic information
- Product Name:
- 2-BROMO-4-CHLOROTHIENO[3,2-C]PYRIDINE
- Synonyms:
-
- 2-BROMO-4-CHLOROTHIENO[3,2-C]PYRIDINE
- 2-broMo-4-chlorothieno[3
- Thieno[3,2-c]pyridine, 2-bromo-4-chloro-
- 2-bromo-4-chlorothieno[3,2-c]pyridine - [B5261]
- CAS:
- 28948-61-0
- MF:
- C7H3BrClNS
- MW:
- 248.53
- Product Categories:
-
- Building Blocks
- Thieno[x,x-y]pyridine
- Heterocycle-Pyridine series
- CHIRAL CHEMICALS
- Mol File:
- 28948-61-0.mol
2-BROMO-4-CHLOROTHIENO[3,2-C]PYRIDINE Chemical Properties
- Melting point:
- 119 °C
- Boiling point:
- 355.2±37.0 °C(Predicted)
- Density
- 1.849±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- solid
- pka
- -1.38±0.40(Predicted)
- color
- Yellow
Safety Information
- Hazard Codes
- Xi
- HS Code
- 2934999090
2-BROMO-4-CHLOROTHIENO[3,2-C]PYRIDINE Usage And Synthesis
Synthesis
28948-60-9
28948-61-0
General procedure for the synthesis of 2-bromo-4-chlorothieno[3,2-C]pyridine from 2-bromo-4-hydroxythieno[3,2-C]pyridine: Phosphorus oxychloride (4.08 g, 26.6 mmol) was slowly added dropwise to a mixture of 2-bromothieno[3,2-c]pyridin-4(5H)-one (2.04 g, 8.87 mmol), and the reaction was carried out at 0 °C. Subsequently, the reaction mixture was heated to 135 °C for 2.5 hours. After completion of the reaction, the mixture was carefully poured onto ice water. The precipitate was collected by filtration and dried to afford 1.78 g (80.7% yield) of the target product 2-bromo-4-chlorothieno[3,2-C]pyridine. The product was characterized by 1H NMR (270 MHz, CH3OH-d4): δ 7.67 (d, 1H), 7.88 (dddd, J = 6.33 Hz, 2H), 8.19 (d, J = 5.54 Hz, 1H); the mass spectrometry (MS) showed the molecular ion peak as 248.0 (M-H)+; and the high-performance liquid chromatography (HPLC) analysis showed the purity as 100%.
References
[1] Patent: WO2004/828, 2003, A1
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