5-BROMO-2-CHLORO-BENZOYL CHLORIDE
5-BROMO-2-CHLORO-BENZOYL CHLORIDE Basic information
- Product Name:
- 5-BROMO-2-CHLORO-BENZOYL CHLORIDE
- Synonyms:
-
- 5-BROMO-2-CHLORO-BENZOYL CHLORIDE
- Benzoyl chloride, 5-bromo-2-chloro-
- Dapagliflozin Impurity 55
- Dapagliflozin Impurity 70
- Dapagliflozin Impurity 70 CRS
- Dapagliflozin Impurity N50
- CAS:
- 21900-52-7
- MF:
- C7H3BrCl2O
- MW:
- 253.91
- Mol File:
- Mol File
5-BROMO-2-CHLORO-BENZOYL CHLORIDE Chemical Properties
- Boiling point:
- 281.4±25.0 °C(Predicted)
- Density
- 1.763±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- White to off-white Solid
5-BROMO-2-CHLORO-BENZOYL CHLORIDE Usage And Synthesis
Uses
5-Bromo-2-chlorobenzoyl Chloride is an intermediate in the synthesis of labelled and unlabelled isotopes of glucuronide metabolites of dapagliflozin. It also functions as an intermediate in the synthesis of dapagliflozin, a potent and selective hSGLT2 inhibitor.
Synthesis
21739-92-4
21900-52-7
Step 1. 5-Bromo-2-chlorobenzoic acid (100 g, 0.43 mol) was dissolved in 500 mL of dichloromethane and 1 g of pyridine was added as a catalyst. Thionyl chloride (60.5 g, 0.51 mol) was added slowly and dropwise at room temperature, followed by heating the reaction mixture to 40 °C and refluxing for 3.5 hours. The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, dichloromethane was removed by distillation under reduced pressure to afford 104 g of 5-bromo-2-chlorobenzoyl chloride (yield: 97%), which can be used directly in the next step of the reaction without further purification.
References
[1] Patent: US2004/138439, 2004, A1. Location in patent: Page 18
[2] Journal of Medicinal Chemistry, 2014, vol. 57, # 4, p. 1236 - 1251
[3] Patent: WO2015/43511, 2015, A1. Location in patent: Paragraph 00227
[4] Patent: CN106892948, 2017, A. Location in patent: Paragraph 0269; 0270; 0271
[5] Patent: CN106316803, 2017, A. Location in patent: Paragraph 0013
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