Trifluoroacetic acid → HCID 58292991, Verbindung

HRID 1947952Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1947952
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(F)(F)F)=O>CO>[CH2:28]([O:27][P:26]([CH:31]([O:32][CH3:40])[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]

Komponenten

5

Edukt 3

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

Produkt 1

HCID 58292991HCID 58292991, VerbindungAusbeute 27,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
105 °C

Versuchsvorschrift

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 MeOH (0.5 mL) was stirred at 105° C. for 45 min in a Biotage microwave reactor. LC-MS showed that the reaction was complete. 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 (18.5 mg, yield: 27%). 1H NMR (CD3OD, 400 MHz): δ=1.21 (dt, J=0.8, 7.2 Hz, 3H), 1.30 (t, J=7.2 Hz, 3H), 2.90 (s, 3H), 3.35 (s, 3H), 3.93-4.14 (m, 4H), 4.61 (d, J=15.2 Hz, 1H), 7.18 (dt, J=1.2, 7.6 Hz, 1H), 7.34 (dd, J=2.0, 8.4 Hz, 2H), 7.49 (dd, J=1.6, 8.4 Hz, 1H), 7.62-7.66 (m, 3H), 8.34 (s, 1H), 8.46 (m, 1H). MS (ES+): m/z 568.11 [MH+]. HPLC: tR=3.31 min (OpenLynx, polar—5 min).

Aufarbeitung

  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)

Quellen und Nachweise

ORD-Eintrag
ord-2635126f5ab440dcbce991370f8db8bb
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08399433B2

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