반응 #921

ord-acf44331951a4df6acd00502ec327265

반응 방정식

[Cl-].[NH4+]
ammonium chloride
[Li][CH2]CCC
n-butyllithium
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1
N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide
CN(C)C(=O)Cl
N,N-dimethylcarbamyl chloride
Cl
HCl
CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
title compound
수율 50.2%
CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
3-[[-(1,1-Dimethylethyl)amino]sulfonyl]-N,N,1-trimethyl-1H-pyrrole-2-carboxamide
수율 50.2%

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added dropwise
  2. 2
    온도to maintain the temperature below -65° C
  3. 3
    온도to warm to room temperature
  4. 4
    workup.STIRRINGstir for ca. 1.5 hours
  5. 5
    온도The reaction mixture was cooled to ca. 5° C.
  6. 6
    workup.STIRRINGThe reaction mixture was stirred for ca. 15 minutes
  7. 7
    기타the aqueous phase was separated from the THF phase
  8. 8
    추출extracted with ethyl acetate
  9. 9
    세척The combined THF and ethyl acetate extracts were washed with brine
  10. 10
    건조dried (MgSO4)
  11. 11
    농축concentrated in vacuo to an oil
  12. 12
    기타The oil was chromatographed on silica with (20% ethyl acetate/80% n-butyl chloride)

실험 절차

To a solution of 6.48 g (30 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 150 mL THF under a nitrogen atmosphere cooled to -78° C. was added dropwise, at such a rate as to keep the temperature below -60° C., 25 mL (61.5 mmol) 2.46M n-butyllithium in hexanes. The reaction mixture was stirred at -78° C. for ca. 30 minutes. To the reaction mixture was added dropwise a solution of 3.1 mL (33 mmol) of N,N-dimethylcarbamyl chloride in 10 mL of THF at such a rate as to maintain the temperature below -65° C. The reaction mixture was allowed to warm to room temperature and stir for ca. 1.5 hours. The reaction mixture was cooled to ca. 5° C. and 60 mL of 50% ammonium chloride solution was added. The reaction mixture was stirred for ca. 15 minutes. The pH was adjusted to ca. 3 with 1N HCl (ca. 30 mL), and the aqueous phase was separated from the THF phase and extracted with ethyl acetate. The combined THF and ethyl acetate extracts were washed with brine, dried (MgSO4) and concentrated in vacuo to an oil. The oil was chromatographed on silica with (20% ethyl acetate/80% n-butyl chloride) affording 4.33 g of the title compound as a pale yellow solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723410uspto-grants-1998_03