Water → N-(3,4-dichlorobenzyl)-N'-1H-indazol-4-ylurea

HRID 585960Notes

Reaction equation

HRID 585960 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:23]=[CH:24][C:25]=1[Cl:26])[CH2:5][NH:6][C:7]([NH:9][C:10]1[CH:18]=[CH:17][CH:16]=[C:15]2[C:11]=1[CH:12]=[N:13][N:14]2C(OC)=O)=[O:8].[OH-].[K+].C(Cl)Cl.O>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH:23]=[CH:24][C:25]=1[Cl:26])[CH2:5][NH:6][C:7]([NH:9][C:10]1[CH:18]=[CH:17][CH:16]=[C:15]2[C:11]=1[CH:12]=[N:13][NH:14]2)=[O:8]

Participants

6

Reactant 4

HCID 962WaterHCID 6344DichloromethaneHCID 14797Potassium HydroxideHCID 22032594Methyl 4-({[(3,4-dichlorobenzyl)amino]carbonyl}amino)-1H-indazole-1-carboxylate

Product 1

HCID 9997058N-(3,4-dichlorobenzyl)-N'-1H-indazol-4-ylurea

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

The product of Example 90C (0.25 g, 0.6 mmol) was heated at reflux in methanol (5 mL) and 0.5N KOH (1 mL) for 0.5 hours. The reaction mixture was allowed to cool to ambient temperature, pH was adjusted to 5, and volume was reduced under reduced pressure. Methylene chloride and water was added, the phases were separated, and the organic phase concentrated under reduced pressure to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ 4.38 (d, 2H), 6.9 (t, 1H), 7.05 (d, 1H), 7.19 (t, 1H), 7.35 (dd, 1H), 7.6 (m, 2H), 8.06 (s, 1H), 8.82 (s, 1H). MS (DCI+) m/z 336 (M+H)+; Anal. Calcd. For C15H13N4Cl2O: C, 53.75; H, 3.62; N, 16.72. Found: C, 53.84, H, 3.44; N, 16.88.

Workup

  1. customthe phases were separated
  2. concentrationthe organic phase concentrated under reduced pressure

Sources & evidence

ORD record
ord-ab9e619de4764ed18d793ea8242e1952
Source dataset
uspto-grants-2005_08
Patent number
US06933311B2

Reaction notes

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