تفاعل #916

ord-1689ec83ac2b4e2e9bc10359a96a617b

معادلة التفاعل

Cn1ccc(S(=O)(=O)NC(C)(C)C)c1
N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide
CN(C)C=O
N,N-dimethylformamide
Cl
HCl
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
title compound
المردود 39.0%
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
N-(1,1-Dimethylethyl)-2-formyl-1-methyl-1H-pyrrole-3-sulfonamide
المردود 39.0%

المذيبات

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added dropwise
  2. 2
    درجة الحرارةto warm to room temperature
  3. 3
    workup.STIRRINGstir for ca. 2 hours
  4. 4
    درجة الحرارةThe reaction mixture was cooled to 0° C.
  5. 5
    أخرىThe THF phase was separated
  6. 6
    غسيلwashed with brine
  7. 7
    تجفيفdried (MgSO4)
  8. 8
    تركيزconcentrated in vacuo
  9. 9
    أخرىThe crude residue was chromatographed on silica (25% ethyl acetate/80% hexanes)

الإجراء التجريبي

To a solution of 12.96 g (60 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 300 mL THF under a nitrogen atmosphere cooled to -78° C. was added dropwise, at such a rate as to keep the temperature below -65° C., 52.35 mL (123 mmol) 2.35M n-butylithium in hexanes. The reaction was stirred at -78° C. for ca. 30 minutes. To the reaction mixture was added 4.64 mL (60 mmol) of N,N-dimethylformamide dropwise. The reaction mixture was allowed to warm to room temperature and stir for ca. 2 hours. The reaction mixture was cooled to 0° C. and acidified with 1N HCl. The THF phase was separated, washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue was chromatographed on silica (25% ethyl acetate/80% hexanes) affording 5.72 g of the title compound as a white solid, m.p. 101.5°-103° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723410uspto-grants-1998_03