反应 #910

反应方程式

HCl

N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide

n-butyllithium

methyl chloroformate

→

title compound

收率 55.9%

Methyl 3-[[(1,1-dimethylethyl)amino]sulfonyl]-1-methyl-1H-pyrrole-2-carboxylate

收率 55.9%

溶剂

THF

—

hexanes

反应条件

后处理

1. 1
   workup.ADDITIONwas added dropwise
2. 2
   温度to warm to room temperature
3. 3
   workup.STIRRINGstir for ca. 1.5 hours
4. 4
   温度was cooled to 0° C.
5. 5
   其他The THF phase was separated
6. 6
   洗涤washed with brine
7. 7
   干燥dried (MgSO4)
8. 8
   浓缩concentrated to an amber oil
9. 9
   其他chromatographed on silica (30% ethyl acetate/70% hexanes)

实验过程

To a solution of 5 g (23 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 150 mL THF under nitrogen atmosphere cooled to -78° C. was added dropwise, at such a rate as to keep the temperature below -65° C., 20 mL (47.4 mmol) 2.32M n-butyllithium in hexanes. The resulting amber turbid solution was stirred at -78° C. for ca. 30 minutes. 1.87 mL (24.3 mmol) of methyl chloroformate was add in one portion and the resulting gold reaction mixture was allowed to warm to room temperature and stir for ca. 1.5 hours. The gold reaction mixture was cooled to 0° C. and acidified with 1N HCl. The THF phase was separated, washed with brine, dried (MgSO4) and concentrated to an amber oil. The oil was combined with the crude product from the previous example and chromatographed on silica (30% ethyl acetate/70% hexanes) affording 3.53 g of the title compound as a solid.

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