Trifluoroacetic acid → [5-(3-Aminomethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amine

HRID 1054390Notes

Reaction equation

HRID 1054390 reaction equation
C(OC(=O)[NH:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([C:15]2[N:20]3[N:21]=[C:22]([NH:24][C:25]4[CH:30]=[CH:29][C:28]([O:31][CH2:32][CH2:33][N:34]5[CH2:38][CH2:37][CH2:36][CH2:35]5)=[CH:27][CH:26]=4)[N:23]=[C:19]3[CH:18]=[CH:17][CH:16]=2)[CH:10]=1)(C)(C)C.FC(F)(F)C(O)=O.C(=O)([O-])O.[Na+]>ClCCl>[NH2:7][CH2:8][C:9]1[CH:10]=[C:11]([C:15]2[N:20]3[N:21]=[C:22]([NH:24][C:25]4[CH:30]=[CH:29][C:28]([O:31][CH2:32][CH2:33][N:34]5[CH2:35][CH2:36][CH2:37][CH2:38]5)=[CH:27][CH:26]=4)[N:23]=[C:19]3[CH:18]=[CH:17][CH:16]=2)[CH:12]=[CH:13][CH:14]=1

Participants

5

Reactant 3

HCID 6422Trifluoroacetic acidHCID 516892Sodium BicarbonateHCID 59590092(3-{2-[4-(2-Pyrrolidin-1-yl-ethoxy)-phenylamino]-[1,2,4]triazolo[1,5-a]pyridin-5-yl}-benzyl)-carbamic acid tert-butyl ester

Product 1

HCID 59589633[5-(3-Aminomethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amine

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

(3-{2-[4-(2-Pyrrolidin-1-yl-ethoxy)-phenylamino]-[1,2,4]triazolo[1,5-a]pyridin-5-yl}-benzyl)-carbamic acid tert-butyl ester (1.78 g, 3.37 mmol) was dissolved in dichloromethane (20 ml). Trifluoroacetic acid (20 ml) was added and the reaction was stirred for 2 hours. Neutralisation was performed by adding saturated aqueous sodium hydrogencarbonate. The aqueous phase was extracted twice with dichloromethane, and the combined organics washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give the desired compound. Yield: 460 mg, 32%. 50 mg was purified by preparatory HPLC.

Workup

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

Sources & evidence

ORD record
ord-6716514dffaf4e81b7e2e6cfcf00683c
Source dataset
uspto-grants-2016_07
Patent number
US09394301B2

Reaction notes

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