3-(Trifluoromethyl)phenol → HCID 59003360, compound

HRID 2267565Notes

Reaction equation

HRID 2267565 reaction equation
Cl[CH2:2][CH2:3][CH2:4][S:5]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[C:22]3[C:17](=[C:18]([C:29]([NH2:31])=[O:30])[CH:19]=[C:20]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[CH:21]=3)[NH:16][CH:15]=2)[CH2:10][CH2:9]1)(=[O:7])=[O:6].[F:32][C:33]([F:42])([F:41])[C:34]1[CH:35]=[C:36]([OH:40])[CH:37]=[CH:38][CH:39]=1.C([O-])([O-])=O.[K+].[K+]>[I-].[Na+]>[C:23]1([C:20]2[CH:21]=[C:22]3[C:17](=[C:18]([C:29]([NH2:31])=[O:30])[CH:19]=2)[NH:16][CH:15]=[C:14]3[CH:11]2[CH2:12][CH2:13][N:8]([S:5]([CH2:4][CH2:3][CH2:2][O:40][C:36]3[CH:37]=[CH:38][CH:39]=[C:34]([C:33]([F:32])([F:41])[F:42])[CH:35]=3)(=[O:7])=[O:6])[CH2:9][CH2:10]2)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1

Participants

5

Reactant 3

HCID 73763-(Trifluoromethyl)phenolHCID 11430Potassium CarbonateHCID 590032803-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamide

Product 1

HCID 59003360HCID 59003360, compoundYield 49.1%

Reagents, catalysts & solvents 1

HCID 5238Sodium IodideCatalyst

Procedure

Following the general procedure of example 159, 3-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamide (40.0 mg, 0.087 mmol), 3-trifluoromethylphenol (162 mg, 0.87 mmol), K2CO3 (35.0 mg, 0.35 mmol) and sodium iodide (0.5 mg) were reacted to give the title compound (25.0 mg, 49%).

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-5435d0e0a8494ade919c6083cf5a190f
Source dataset
uspto-grants-2010_12
Patent number
US07858796B2

Reaction notes

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