Trifluoroacetic acid → HCID 58292903, compound

HRID 1947951Notes

Reaction equation

HRID 1947951 reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:18]=[CH:17][CH:16]=[CH:15][C:10]=2[C:11]([NH:13][CH3:14])=[O:12])[C:5]([C:19]([F:22])([F:21])[F:20])=[CH:4][N:3]=1.[CH2:23]([O:25][P:26]([CH:31]([C:33]1[CH:38]=[CH:37][C:36]([NH2:39])=[CH:35][CH:34]=1)[OH:32])(=[O:30])[O:27][CH2:28][CH3:29])[CH3:24].[C:40](O)([C:42](F)(F)F)=O>CCO>[CH2:28]([O:27][P:26]([CH:31]([O:32][CH2:40][CH3:42])[C:33]1[CH:34]=[CH:35][C:36]([NH:39][C:2]2[N:7]=[C:6]([NH:8][C:9]3[CH:18]=[CH:17][CH:16]=[CH:15][C:10]=3[C:11](=[O:12])[NH:13][CH3:14])[C:5]([C:19]([F:22])([F:21])[F:20])=[CH:4][N:3]=2)=[CH:37][CH:38]=1)(=[O:30])[O:25][CH2:23][CH3:24])[CH3:29]

Participants

5

Reactant 3

HCID 6422Trifluoroacetic acidHCID 23061737Diethyl P-[(4-aminophenyl)hydroxymethyl]phosphonateHCID 866338612-((2-Chloro-5-(trifluoromethyl)pyrimidin-4-yl)amino)-N-methylbenzamide

Product 1

HCID 58292903HCID 58292903, compoundYield 12%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
105 °C

Procedure

Under N2, a solution of 2-{[2-chloro-5-(trifluoromethyl)pyrimidin-4-yl]amino}-N-methylbenzamide (40.0 mg, 0.12 mmol) and diethyl[(4-aminophenyl)(hydroxy)methyl]-phosphonate (37.6 mg, 0.15 mmol) in a mixture of TFA (28 uL, 0.36 mmol) and EtOH (0.5 mL) was stirred at 105° C. for 45 min in a Biotage microwave reactor. The solvents were removed under reduced pressure and to the residue was added sat. NaHCO3 (aq) (2 mL) and DCM (5 mL). Layers were separated and the aqueous layer was extracted with DCM (3×5 mL). The combined organic phases were dried over MgSO4, concentrated, and purified by silica gel chromatography (5% 7 N NH3 in MeOH in DCM) to afford the desired product as a white-colored solid (8.4 mg, yield: 12%). 1H NMR (CD3OD, 400 MHz): δ=1.22 (dt, J=0.8, 7.6 Hz, 6H), 1.30 (t, J=7.2 Hz, 3H), 2.90 (s, 3H), 3.47-3.57 (m, 2H), 3.95-4.15 (m, 4H), 4.72 (d, J=16.0 Hz, 1H), 7.18 (dt, J=1.2, 7.6 Hz, 1H), 7.35 (dd, J=2.0, 8.4 Hz, 2H), 7.49 (dd, J=1.6, 8.8 Hz, 1H), 7.63-7.65 (m, 3H), 8.34 (s, 1H), 8.45 (m, 1H). MS (ES+): m/z 582.17 [MH+] HPLC: tR=3.44 min (OpenLynx, polar—5 min).

Workup

  1. customThe solvents were removed under reduced pressure and to the residue
  2. additionwas added sat. NaHCO3 (aq) (2 mL) and DCM (5 mL)
  3. customLayers were separated
  4. extractionthe aqueous layer was extracted with DCM (3×5 mL)
  5. dry with materialThe combined organic phases were dried over MgSO4
  6. concentrationconcentrated
  7. custompurified by silica gel chromatography (5% 7 N NH3 in MeOH in DCM)

Sources & evidence

ORD record
ord-62090c4927864e5dbc529843773c9c27
Source dataset
uspto-grants-2013_03
Patent number
US08399433B2

Reaction notes

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