2-Chloro-6-methylaniline → 7-chloro-1H-indazole

HRID 334638Notes

Reaction equation

HRID 334638 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH2:9].[N:10]([O-])=O.[Na+].C([O-])(=O)C.[Na+]>OS(O)(=O)=O.O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:3]=1[NH:9][N:10]=[CH:8]2

Participants

6

Conditions

Temperature
7.5 °C

Procedure

A solution of 2-chloro-6-methyl-phenylamine (500 mg, 3.53 mmol) in H2SO4 (1.37 mL) was diluted by adding over 15 min. 2 mL of water in order to maintain a temperature below 90° C. Then the reaction mixture was cooled to 5-10° C. and a solution of sodium nitrite (246 mg, 3.57 mmol) in water (1 mL) was added over 2 hours. The resulting diazonium solution was then added to a solution of sodium acetate (5.21 g, 63.6 mmol) in water (20 mL) at a temperature maintained between 65 to 75° C. The resulting precipitate was filtered and treated with a solution of NaOH (6.00 g) in water (100 mL) at 95-100° C. The aqueous phase was separated while hot from the small amount of black tarry by-products, cooled to 50-60° C. and acidified with HCl (37%, 12.5 mL). The reaction mixture was cooled down to room temperature, the resulting precipitate was filtered, was washed thrice with cold water and was dried under vacuum to yield 7-chloro-1H-indazole (220 mg, 1.44 mmol, 41%) as a white solid.

Workup

  1. additionby adding over 15 min
  2. temperaturemaintained between 65 to 75° C
  3. filtrationThe resulting precipitate was filtered
  4. additiontreated with a solution of NaOH (6.00 g) in water (100 mL) at 95-100° C
  5. customThe aqueous phase was separated while hot from the small amount of black tarry by-products
  6. temperaturecooled to 50-60° C.
  7. temperatureThe reaction mixture was cooled down to room temperature
  8. filtrationthe resulting precipitate was filtered
  9. washwas washed thrice with cold water
  10. customwas dried under vacuum

Sources & evidence

ORD record
ord-c8ae5b2e49c64cb1bd87c65406178cfa
Source dataset
uspto-grants-2014_11
Patent number
US08883826B2

Reaction notes

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