تفاعل #595377

ord-21d16a97bfb642ac841ff566818ce3a4

معادلة التفاعل

O=S(=O)(Cl)c1ccccc1Cl
2-chlorobenzenesulfonyl chloride
Brc1n[nH]c2ccncc12
3-bromo-1H-pyrazolo[4,3-c]pyridine
[H-].[Na+]
sodium hydride
O=S(=O)(c1ccccc1Cl)n1nc(Br)c2cnccc21
3-bromo-1-(2-chlorophenylsulfonyl)-1H-pyrazolo[4,3-c]pyridine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    أخرىThe reaction mixture was quenched by the addition of water
  3. 3
    استخلاصThe product was extracted into ethyl acetate
  4. 4
    غسيلthe organic layer was washed with brine
  5. 5
    أخرىThe organic solvent was evaporated under reduced pressure

الإجراء التجريبي

To a solution of 3-bromo-1H-pyrazolo[4,3-c]pyridine (198 mg, 1,0 mmol) in 10 ml THF was added portion wise at 0° C. sodium hydride (101 mg, 4 mmol, 95%). After addition was complete, 2-chlorobenzenesulfonyl chloride (495 mg, 2.347 mmol) was added and the reaction mixture was stirred overnight at room temperature. The reaction mixture was quenched by the addition of water. The product was extracted into ethyl acetate and the organic layer was washed with brine. The organic solvent was evaporated under reduced pressure to give 3-bromo-1-(2-chlorophenylsulfonyl)-1H-pyrazolo[4,3-c]pyridine as a yellow oil. The product was used in the next step without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09095583B2uspto-grants-2015_08