Trifluoroacetic acid → HCID 86692547, compound

HRID 1748593Notes

Reaction equation

HRID 1748593 reaction equation
C(OC([N:8]1[CH2:13][CH:12]=[C:11]([C:14]2[N:19]=[CH:18][C:17]([NH:20][C:21]([C:23]3[CH:24]=[N:25][N:26]([C:29]4[CH:34]=[CH:33][C:32]([C:35]([F:38])([F:37])[F:36])=[CH:31][N:30]=4)[C:27]=3[CH3:28])=[O:22])=[CH:16][CH:15]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.FC(F)(F)C(O)=O.[OH-].[Na+]>ClCCl>[CH3:28][C:27]1[N:26]([C:29]2[CH:34]=[CH:33][C:32]([C:35]([F:37])([F:36])[F:38])=[CH:31][N:30]=2)[N:25]=[CH:24][C:23]=1[C:21]([NH:20][C:17]1[CH:18]=[N:19][C:14]([C:11]2[CH2:12][CH2:13][NH:8][CH2:9][CH:10]=2)=[CH:15][CH:16]=1)=[O:22]

Participants

5

Reactant 3

HCID 6422Trifluoroacetic acidHCID 14798Sodium HydroxideHCID 86692545HCID 86692545, compound

Product 1

HCID 86692547HCID 86692547, compoundYield 62.9%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To N-[6-(1-tert-butyloxycarbonyl-1,2,3,6-tetrahydropyridin-4-yl)pyridin-3-yl]-5-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-carboxamide (3.53 g) were added dichloromethane (70 ml) and trifluoroacetic acid (14 ml), and stirred at room temperature for 4.5 hours. To the reaction solution was added 4 N aqueous solution of sodium hydroxide under ice-cooling, and the precipitated solid was purified with basic silica gel chromatography (chloroform/methanol) to give the titled compound (1.8 g) as a yellow solid. MS (ESI) m/z: 429 (M+H)+.

Workup

  1. temperaturecooling
  2. customthe precipitated solid was purified with basic silica gel chromatography (chloroform/methanol)

Sources & evidence

ORD record
ord-5996cff741154752b80166a4e6e28293
Source dataset
uspto-grants-2015_10
Patent number
US09150555B2

Reaction notes

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