Phosphorus pentachloride → HCID 54498860, compound

HRID 1463220Notes

Reaction equation

HRID 1463220 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 The filter cake
  3. washis washed with toluene
  4. filtrationfiltered

Sources & evidence

ORD record
ord-21c6060097b64a3e88cd08097b0904be
Source dataset
uspto-grants-1994_04
Patent number
US05300479

Reaction notes

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