Dichloromethane → HCID 86699600, compound

HRID 2400645Notes

Reaction equation

HRID 2400645 reaction equation
[C:1]([O:5][C:6](=[O:26])[NH:7][S:8](=[O:25])(=[O:24])[NH:9][CH2:10][CH2:11][O:12][N:13]1C(=O)C2C(=CC=CC=2)C1=O)([CH3:4])([CH3:3])[CH3:2].C(Cl)Cl.O.NN>C(O)C>[NH2:13][O:12][CH2:11][CH2:10][NH:9][S:8]([NH:7][C:6](=[O:26])[O:5][C:1]([CH3:3])([CH3:2])[CH3:4])(=[O:25])=[O:24]

Participants

5

Reactant 3

HCID 6344DichloromethaneHCID 24654Hydrazine hydrate (1:1)HCID 86699599HCID 86699599, compound

Product 1

HCID 86699600HCID 86699600, compoundYield 44%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a mixture of tert-butyl({2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]ethyl}sulfamoyl)carbamate 77 (0.62 g, 1.61 mmol) in a solution of DCM (10 mL) and ethanol (2 mL) was added hydrazine hydrate (0.092 mL, 1.61 mmol) at room temperature. The mixture was stirred at room temperature overnight, filtered and concentrated to provide a residue which was subjected to chromatography to give 78 (0.18 g, 44%) as a white solid.

Workup

  1. filtrationfiltered
  2. concentrationconcentrated
  3. customto provide a residue which

Sources & evidence

ORD record
ord-da7540b5fe7046a090546537dd935426
Source dataset
uspto-grants-2014_08
Patent number
US08796257B2

Reaction notes

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