تفاعل #2028943

ord-0ef032fbd36b45baaf19e2282c78c62b

معادلة التفاعل

CS(=O)(=O)Nc1ccc(Br)c(Cl)c1
N-(4-bromo-3-chlorophenyl)methanesulfonamide
OB(O)c1ccc(Cl)c(F)c1
4-chloro-3-fluorophenylboronic acid
CS(=O)(=O)Nc1ccc(-c2ccc(Cl)c(F)c2)c(Cl)c1
desired product
CS(=O)(=O)Nc1ccc(-c2ccc(Cl)c(F)c2)c(Cl)c1
N-(2,4′-dichloro-3′-fluorobiphenyl-4-yl)methanesulfonamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was heated under reflux conditions for 1 hours
  2. 2
    ترشيحThe mixture was filtered through Celite (3 g)
  3. 3
    غسيلthe Celite was washed with EtOAc (70 mL)
  4. 4
    أخرىThe solvent was removed under a reduced pressure
  5. 5
    أخرىObtained crude mixture
  6. 6
    أخرىwas purified by column chromatography (SiO2=80 g, EtOAc/hexane=1:3˜1:1, Rf=0.4)

الإجراء التجريبي

N-(4-bromo-3-chlorophenyl)methanesulfonamide (B, 100.0 mg, 0.351 mmol), 4-chloro-3-fluorophenylboronic acid (73.4 mg, 0.421 mmol, L2 equiv.) and Pd(PPh3)4 (20.3 mg, 0.0176 mmol, 0.05 equiv.) was placed in a 50 mL round bottomed flask under a nitrogen atmosphere. To the flask were added 2M-Na1CO3 (1.0 mL, 2.0 mmol, 5.7 equiv.) and DME (4 mL) subsequently at ambient temperature. The mixture was heated under reflux conditions for 1 hours. The mixture was filtered through Celite (3 g) and the Celite was washed with EtOAc (70 mL). The solvent was removed under a reduced pressure. Obtained crude mixture was purified by column chromatography (SiO2=80 g, EtOAc/hexane=1:3˜1:1, Rf=0.4) to give the desired product as colorless crystals (compound 5 (designated PT-017).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08389500B2uspto-grants-2013_03