Реакция #84790

Уравнение реакции

potassium 2-methoxy-2-(4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)phenyl)acetate

diisopropylethylamine

bis(2-methoxyethyl)aminosulfur trifluoride

N,O-dimethylhydroxylamine hydrochloride

→

N,2-dimethoxy-N-methyl-2-(4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)phenyl)acetamide

Выход 37.5%

Растворители

H2O

DMF

Условия реакции

Обработка

1. 1
   workup.STIRRINGAfter stirring for a further 15 min over an ice bath
2. 2
   workup.STIRRINGstirred for 3.5 hrs
3. 3
   Экстракцияthe mixture was extracted with EtOAc
4. 4
   ПромывкаThe combined organics were washed with H2O, saturated aqueous NH4Cl, saturated aqueous NaHCO3, and brine
5. 5
   Сушкаthen dried over Na2SO4
6. 6
   Концентрированиеconcentrated in vacuo
7. 7
   ДругоеPurification by chromatography (45-90% EtOAc-hexanes; EtOAc containing 1% Et3N)

Методика

To an ice-cold solution of potassium 2-methoxy-2-(4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)phenyl)acetate (1.25 g, 2.1 mmol) in anhydrous DMF (10 mL) under argon was added diisopropylethylamine (0.54 mL, 3.1 mmol) and bis(2-methoxyethyl)aminosulfur trifluoride (0.46 mL, 2.5 mmol) dropwise. The reaction was stirred for 30 min then N,O-dimethylhydroxylamine hydrochloride (0.303 g, 3.1 mmol) was added. After stirring for a further 15 min over an ice bath, the mixture was allowed to warm to room temperature and stirred for 3.5 hrs. H2O was added and the mixture was extracted with EtOAc. The combined organics were washed with H2O, saturated aqueous NH4Cl, saturated aqueous NaHCO3, and brine then dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (45-90% EtOAc-hexanes; EtOAc containing 1% Et3N) to give N,2-dimethoxy-N-methyl-2-(4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)phenyl)acetamide (0.478 g from two reactions, 32% yield overall).

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