Phosphorus pentachloride → HCID 54498860, compound

HRID 1031029Notes

Reaction equation

HRID 1031029 reaction equation
[C:1]([C:4]([NH:9][C:10]([C:12]1[C:20]([C:21]([O:23][CH3:24])=[O:22])=[CH:19][CH:18]=[C:17]2[C:13]=1[C:14]([CH3:26])=[N:15][N:16]2[CH3:25])=O)([CH3:8])[CH:5]([CH3:7])[CH3:6])(=[O:3])[NH2:2].P(Cl)(Cl)(Cl)(Cl)Cl.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[CH:5]([C:4]1([CH3:8])[C:1](=[O:3])[NH:2][C:10]([C:12]2[C:20]([C:21]([O:23][CH3:24])=[O:22])=[CH:19][CH:18]=[C:17]3[C:13]=2[C:14]([CH3:26])=[N:15][N:16]3[CH3:25])=[N:9]1)([CH3:7])[CH3:6]

Participants

5

Conditions

Temperature
90 °C

Procedure

A mixture of methyl 4-[(1-carbamoyl-1,2-dimethylpropyl)carbamoyl]-1,3-dimethyl-1H-indazole-5-carboxylate (0.600 g, 1.67 mmol), phosphorus pentachloride (1.04 g, 5.00 mmol) and dry toluene (7.0 mL) is stirred for 3.5 hours at 90° C. cooled and filtered. The filter cake is washed with toluene, slurried in water, treated with sodium bicarbonate (0.370 g, 4.40 mmol) to pH 8.5 and filtered to afford the title product as a white solid (0.490 g, 85.7%), mp 130°-150° C.

Workup

  1. temperaturecooled
  2. filtrationfiltered
  3. washThe filter cake is washed with toluene
  4. filtrationfiltered

Sources & evidence

ORD record
ord-1cc1e7ece5154e9fb51aeb448a4e46ed
Source dataset
uspto-grants-1992_04
Patent number
US05108485

Reaction notes

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