1-Tert-butyl-4-(isothiocyanatomethyl)benzene → N-(4-t-Butylbenzyl)-N'-{1-methyl-1-[4-(methylsulfonylamino)phenyl]ethyl}thiourea

HRID 238941Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 238941
[CH3:1][C:2]([NH:15]C(=O)OCC1C=CC=CC=1)([C:4]1[CH:9]=[CH:8][C:7]([NH:10][S:11]([CH3:14])(=[O:13])=[O:12])=[CH:6][CH:5]=1)[CH3:3].[H][H].[C:28]([C:32]1[CH:41]=[CH:40][C:35]([CH2:36][N:37]=[C:38]=[S:39])=[CH:34][CH:33]=1)([CH3:31])([CH3:30])[CH3:29]>[Pd].CO>[C:28]([C:32]1[CH:41]=[CH:40][C:35]([CH2:36][NH:37][C:38]([NH:15][C:2]([CH3:3])([C:4]2[CH:5]=[CH:6][C:7]([NH:10][S:11]([CH3:14])(=[O:13])=[O:12])=[CH:8][CH:9]=2)[CH3:1])=[S:39])=[CH:34][CH:33]=1)([CH3:31])([CH3:29])[CH3:30]

Komponenten

6

Versuchsvorschrift

A suspension of Benzyl N-{1-Methyl-1-[4-(methylsulfonylamino)phenyl]ethyl}carbamate (21-1, 0.5 mmol) and 5% palladium on carbon (100 mg) in MeOH (10 mL) was hydrogenated under a rubber balloon of hydrogen for 1 h. After the solvent was evaporated by rotary evaporator, the residue was dissolved in DMF (5 mL) and treated with 4-t-butylbenzyl isothiocyanate (0.5 mmol). After being stirred overnight, the mixture went to aqueous work-up and the residue was purified by column chromatography on silica gel with EtOAc:hexanes as eluant to afford N-(4-t-Butylbenzyl)-N′-{1-methyl-1-[4-(methylsulfonylamino)phenyl]ethyl}thiourea (21-7, CHK-593)

Aufarbeitung

  1. customAfter the solvent was evaporated by rotary evaporator
  2. dissolutionthe residue was dissolved in DMF (5 mL)
  3. customthe residue was purified by column chromatography on silica gel with EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-79e35091780e4bd38f026607a396788d
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08642657B2

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