Trifluoroacetic acid → Ammonium Acetate

HRID 2068367Notes

Reaction equation

HRID 2068367 reaction equation
[F:1][C:2]1[N:7]2[N:8]=[C:9]([C:22]3[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=3)[C:10]([C:11]([N:13](C)[C:14](=O)OC(C)(C)C)=[O:12])=[C:6]2[CH:5]=[C:4]([C:29]2[CH:34]=[C:33]([C:35](=[O:46])[NH:36][C:37]3([C:40]4[CH:45]=[CH:44][CH:43]=[CH:42][N:41]=4)[CH2:39][CH2:38]3)[CH:32]=[CH:31][C:30]=2[CH3:47])[CH:3]=1.[C:48]([OH:54])([C:50](F)(F)F)=[O:49]>ClCCl>[C:48]([O-:54])(=[O:49])[CH3:50].[NH4+:7].[F:1][C:2]1[N:7]2[N:8]=[C:9]([C:22]3[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=3)[C:10]([C:11]([NH:13][CH3:14])=[O:12])=[C:6]2[CH:5]=[C:4]([C:29]2[CH:34]=[C:33]([C:35](=[O:46])[NH:36][C:37]3([C:40]4[CH:45]=[CH:44][CH:43]=[CH:42][N:41]=4)[CH2:38][CH2:39]3)[CH:32]=[CH:31][C:30]=2[CH3:47])[CH:3]=1

Participants

5

Reactant 2

HCID 6422Trifluoroacetic acidHCID 59233755Tert-butyl 7-fluoro-2-(4-fluorophenyl)-5-(2-methyl-5-(1-(pyridin-2-yl)cyclopropylcarbamoyl)phenyl)pyrazolo[1,5-a]pyridine-3-carbonyl(methyl)carbamate

Product 2

HCID 517165Ammonium AcetateHCID 592338207-fluoro-2-(4-fluorophenyl)-N-methyl-5-(2-methyl-5-(1-(pyridin-2-yl)cyclopropylcarbamoyl)phenyl)pyrazolo[1,5-a]pyridine-3-carboxamide

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution containing tert-butyl 7-fluoro-2-(4-fluorophenyl)-5-(2-methyl-5-(1-(pyridin-2-yl)cyclopropylcarbamoyl)phenyl)pyrazolo[1,5-a]pyridine-3-carbonyl(methyl)carbamate (0.022 g, 0.035 mmol) and dichloromethane (3.0 mL) was added TFA (0.22 mL, 2.8 mmol) at room temperature. The solution was maintained for 15 min at room temperature and concentrated to dryness. The residue thus obtained was purified using preparative HPLC (Waters-Xbridge, 50×100 mm, 5 micron, C18 column; 0.1M ammonium acetate, 10-100% B (B=5% H2O/CH3CN)/A (A=95% H2O/CH3CN), 15 min. gradient) to afford 7-fluoro-2-(4-fluorophenyl)-N-methyl-5-(2-methyl-5-(1-(pyridin-2-yl)cyclopropylcarbamoyl)phenyl)pyrazolo[1,5-a]pyridine-3-carboxamide as a white solid. Preparative HPLC retention time: 9.0 min. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.44-8.54 (m, 1H), 8.18 (d, J=1.51 Hz, 1H), 7.79-7.85 (m, 2H), 7.72-7.78 (m, 2H), 7.61 (td, J=7.78, 1.76 Hz, 1H), 7.41 (dd, J=8.03, 3.26 Hz, 2H), 7.22-7.32 (m, 2H), 7.20 (s, 1H), 7.08 (ddd, J=7.40, 4.89, 1.25 Hz, 1H), 6.69 (dd, J=5.65, 1.63 Hz, 1H), 5.58 (d, J=4.52 Hz, 1H), 2.87 (d, J=5.02 Hz, 3H), 2.42 (s, 3H), 1.67-1.78 (m, 2H), 1.39-1.48 (m, 2H). LCMS retention time: 1.873 min. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Phenomenex-Luna, 10 micron, C18, 3.0×50 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 4 mL/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 3 min, a hold time of 1 min, and an analysis time of 4 min where solvent A was 10% CH3OH/90% H2O/10 mM TFA and solvent B was 10% H2O/90% CH3OH/10 mM TFA. MS data was determined using a Micromass Platform for LC in electrospray mode. m/z 538 (MH+).

Workup

  1. concentrationconcentrated to dryness
  2. customThe residue thus obtained
  3. customwas purified

Sources & evidence

ORD record
ord-9e69ae383af54982a456f2149b3f2fb3
Source dataset
uspto-grants-2012_10
Patent number
US08293909B2

Reaction notes

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