Trifluoroacetic acid → HCID 59590052, compound

HRID 1472835Notes

Reaction equation

HRID 1472835 reaction equation
COC1C=CC([O:7][C:8]2[CH:9]=[C:10]([C:14]3[N:19]4[N:20]=[C:21]([NH:23][C:24]5[CH:29]=[CH:28][C:27]([O:30][CH2:31][CH2:32][N:33]6[CH2:37][CH2:36][CH2:35][CH2:34]6)=[CH:26][CH:25]=5)[N:22]=[C:18]4[CH:17]=[CH:16][CH:15]=3)[CH:11]=[CH:12][CH:13]=2)=CC=1.FC(F)(F)C(O)=O.C(=O)([O-])O.[Na+]>ClCCl>[N:33]1([CH2:32][CH2:31][O:30][C:27]2[CH:28]=[CH:29][C:24]([NH:23][C:21]3[N:22]=[C:18]4[CH:17]=[CH:16][CH:15]=[C:14]([C:10]5[CH:9]=[C:8]([OH:7])[CH:13]=[CH:12][CH:11]=5)[N:19]4[N:20]=3)=[CH:25][CH:26]=2)[CH2:34][CH2:35][CH2:36][CH2:37]1

Participants

5

Procedure

{5-[3-(4-Methoxy-phenoxy)-phenyl]-[1,2,4]triazolo[1,5-a]pyridin-2-yl}-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amine (2.90 g, 5.41 mmol) was dissolved in dichloromethane (10 ml). Trifluoroacetic acid (10 ml) was added and the reaction mixture stirred for 2 hours. Neutralisation was performed by adding saturated aqueous sodium hydrogencarbonate. The aqueous was extracted twice with dichloromethane, then the combined organics were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give the desired compound. Yield 2.01 g, 89%. 50 mg was purified by preparatory HPLC.

Workup

  1. extractionThe aqueous was extracted twice with dichloromethane
  2. washthe combined organics were washed with brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-8af2835d7720468c8c7b4938bdf9032e
Source dataset
uspto-grants-2015_04
Patent number
US09012633B2

Reaction notes

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