Dichloromethane → 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide

HRID 52297

Reaktionsgleichung

Reaktionsgleichung von HRID 52297
F[C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.C[Al](C)C.[CH3:13][S:14]([C:17]1[CH:24]=[CH:23][C:20]([C:21]#[N:22])=[CH:19][CH:18]=1)(=[O:16])=[O:15].C(Cl)[Cl:26]>C1(C)C=CC=CC=1.C(Cl)(Cl)Cl>[CH3:13][S:14]([C:17]1[CH:24]=[CH:23][C:20]([C:21](=[NH:22])[NH:6][C:5]2[CH:7]=[CH:8][C:2]([Cl:26])=[CH:3][CH:4]=2)=[CH:19][CH:18]=1)(=[O:15])=[O:16]

Komponenten

7

Edukt 4

HCID 6344DichloromethaneHCID 97314-FluoroanilineHCID 5199814-(Methylsulfonyl)benzonitrileHCID 16682925Trimethylaluminum

Produkt 1

HCID 1785047634-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamideAusbeute 35 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1140TolueneLösungsmittelHCID 6212ChloroformLösungsmittel

Versuchsvorschrift

To a suspension of 4-fluoroaniline (4 mL, 40 mmol) in toluene (120 mL), trimethylaluminum (2M solution in toluene, 21 mL, 42 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 3 hours. A solution of 4-(methylsulfonyl)benzonitrile (7.65 g, 40 mmol) in methylene chloride (100 mL) was added over 10 minutes and the reaction mixture was heated to 70°-75° C. After 48 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol. The combined filtrates were concentrated in vacuo and the resulting crude intermediate (7.7 g) was chromatographed [silica gel, hexane/ethyl acetate, 25/75] to give 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide (4.1 g, 35%) as a white solid: mp (DSC) 182° C. Anal. Calc'd. for C14H13N2SO2F: C, 57.52, H, 4.48, N, 9.58, S, 10.97. Found: C, 57.37, H, 4.69, N, 9.21, S, 10.69.

Aufarbeitung

  1. additionwas added over 15 minutes
  2. temperaturethe reaction mixture was heated to 70°-75° C
  3. waitAfter 48 hours
  4. temperaturethe reaction mixture was cooled to room temperature
  5. filtrationAfter filtration
  6. washthe residue was washed with a mixture of methylene chloride/methanol
  7. concentrationThe combined filtrates were concentrated in vacuo
  8. customthe resulting crude intermediate (7.7 g) was chromatographed [silica gel, hexane/ethyl acetate, 25/75]

Quellen und Nachweise

ORD-Eintrag
ord-79d9344789514a02b4037e46ddef742f
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05616601

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