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6-BROMO-5-METHYL (1H)INDAZOLE

Basic information Uses Safety Supplier Related

6-BROMO-5-METHYL (1H)INDAZOLE Basic information

Product Name:
6-BROMO-5-METHYL (1H)INDAZOLE
Synonyms:
  • 6-BROMO-5-METHYL (1H)INDAZOLE
  • 1H-Indazole, 6-broMo-5-Methyl-
  • 6-broMo-5-Methyl indazole
  • 7-(Methanesulfonyl)ethylsuccinimidyl
CAS:
1000343-69-0
MF:
C8H7BrN2
MW:
211.06
Product Categories:
  • Indazoles
  • Building Blocks
  • Indazole
Mol File:
Mol File
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6-BROMO-5-METHYL (1H)INDAZOLE Chemical Properties

Boiling point:
344.6±22.0 °C(Predicted)
Density 
1.654
storage temp. 
2-8°C(protect from light)
pka
13.01±0.40(Predicted)
form 
powder
color 
Yellow
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HS Code 
2933998090
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6-BROMO-5-METHYL (1H)INDAZOLE Usage And Synthesis

Uses

6-Bromo-5-chloro-1H-indazole is a fine chemical raw material that can be used as a pharmaceutical intermediate.

Synthesis

69383-60-4

1000343-69-0

The general procedure for the synthesis of 6-bromo-5-methyl-1H-indazole from 5-bromo-2,4-dimethylaniline was as follows: to a solution of 5-bromo-2,4-dimethylaniline (15.09 g, 75.0 mmol) in chloroform (150 mL) was added sequentially, under ice-bath conditions, acetic anhydride (Ac2O, 15.0 g, 150 mmol), potassium acetate (KOAc. 8.009 g, 82.5 mmol), 18-crown-6 (10.0 g, 37.5 mmol) and isoamyl nitrite (26.3 g, 225 mmol). The reaction mixture was heated to reflux for 36 hours. After completion of the reaction, the reaction mixture was concentrated and the residue was dissolved in ethyl acetate (EtOAc, 500 mL). The organic phase was washed with water (100 mL), dried over anhydrous sodium sulfate (Na2SO4) and concentrated. The residue was dissolved in tetrahydrofuran (THF, 100 mL) and sodium hydroxide solution (4 M, 40.0 mL, 160 mmol) was added. After stirring for 1 h at room temperature, the solvent was removed under reduced pressure. The residue was partitioned between ethyl acetate (400 mL) and water (200 mL). The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. The crude product was purified by column chromatography (petroleum ether: ethyl acetate, gradient elution from 10:1 to 5:1) to afford 6-bromo-5-methyl-1H-indazole (5.1 g, 32% yield) as an orange solid.1H NMR (300 MHz, CDCl3): δ 10.20 (brs, 1H), 7.99 (s, 1H), 7.75 (s, 1H) 7.61 (s, 1H), 2.50 (s, 3H).

References

[1] Patent: WO2017/12576, 2017, A1. Location in patent: Page/Page column 68
[2] Patent: WO2018/137619, 2018, A1. Location in patent: Page/Page column 52; 53; 57; 58; 76
[3] Patent: WO2018/137618, 2018, A1. Location in patent: Page/Page column 50; 60; 61
[4] Patent: WO2018/137573, 2018, A1. Location in patent: Page/Page column 45; 46
[5] Patent: WO2018/137607, 2018, A1. Location in patent: Page/Page column 42-43

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