Water → methyl 4-nitro-1H-indazole-1-carboxylate

HRID 586064Notes

Reaction equation

HRID 586064 reaction equation
[H-].[Na+].[N+:3]([C:6]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:7]=1[CH:8]=[N:9][NH:10]2)([O-:5])=[O:4].Cl[C:16]([O:18][CH3:19])=[O:17].O>CN(C=O)C>[N+:3]([C:6]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:7]=1[CH:8]=[N:9][N:10]2[C:16]([O:18][CH3:19])=[O:17])([O-:5])=[O:4]

Participants

6

Procedure

NaH (0.3 g, 12.5 mmol) in DMF (5 mL) was treated with 4-nitro-1H-indazole (1.33 g, 10 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and stir for 1 hour. The mixture was treated with methyl chloroformate (0.9 mL) and stirred at room temperature for 3 hours. The mixture was treated with water and filtered to provide the title compound as a solid. 1H NMR (300 MHz, DMSO-d6) δ 4.1 9 (s, 3H), 7.9 (t, 1H), 8.38 (d, 1H), 8.62 (d, 1H), 8.85 (s, 1H).

Workup

  1. stirringstirred at room temperature for 3 hours
  2. filtrationfiltered

Sources & evidence

ORD record
ord-da5f5e15cde44a4080deeedc511fab57
Source dataset
uspto-grants-2005_08
Patent number
US06933311B2

Reaction notes

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