Hydrogen Peroxide → HCID 178513683, compound

HRID 1452475Notes

Reaction equation

HRID 1452475 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([N:13]2[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]3[CH2:26][CH2:25][C@H:24]([NH:27][S:28]([C:31]4[CH:32]=[N:33][CH:34]=[CH:35][CH:36]=4)(=[O:30])=[O:29])[CH2:23][CH2:22]3)[CH2:15][CH2:14]2)[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1)#[N:2].C([O-])([O-])=[O:38].[K+].[K+].OO.O>CS(C)=O>[NH2:2][C:1]([C:3]1[CH:4]=[C:5]([N:13]2[CH2:14][CH2:15][N:16]([CH2:19][CH2:20][C@H:21]3[CH2:26][CH2:25][C@H:24]([NH:27][S:28]([C:31]4[CH:32]=[N:33][CH:34]=[CH:35][CH:36]=4)(=[O:30])=[O:29])[CH2:23][CH2:22]3)[CH2:17][CH2:18]2)[CH:6]=[C:7]([C:9]([F:10])([F:11])[F:12])[CH:8]=1)=[O:38]

Participants

6

Procedure

0.37 g (0.7 mmol) of trans-N-(4-{2-[4-(3-cyano-5-trifluoromethyl-phenyl)-piperazin-1-yl]-ethyl}-cyclohexyl)-pyridine-3-sulfonamide was dissolved in 2 ml dimethylsulfoxide, 80 mg K2CO3 was added and 0.15 ml of 30% H2O2 was dropped in while keeping the temperature at 20° C. After stirring for 2 h 20 ml of water was added, the precipitate filtered, washed with water giving the title compound, melting point:191° C. (0.2 g; 53%).

Workup

  1. customat 20° C
  2. additionwas added
  3. filtrationthe precipitate filtered
  4. washwashed with water giving the title compound, melting point:191° C. (0.2 g; 53%)

Sources & evidence

ORD record
ord-393a76f192db482c834fe1d5c554cf8f
Source dataset
uspto-grants-2009_01
Patent number
US07473692B2

Reaction notes

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