반응 #978663

반응 방정식

diisopropylethylamine

4-acetylthio-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)piperidine

hydrazine acetate

sodium hydrogencarbonate

p-nitrobenzyl (1R,5S,6S)-2-diphenylphosphoryloxy-6-[(R)-1-hydroxyethyl]-1-methylcarbapen-2-em-3-carboxylate

→

p-nitrobenzyl (1R,5S,6S)-2-[1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)piperidin-4-yl]thio-6-[(R)-1-hydroxyethyl]-1-methylcarbapen-2-em-3-carboxylate

수율 38.0%

용매

dimethylformamide

ethyl acetate

acetonitrile

반응 조건

후처리

1. 1
   기타the completion of the reaction
2. 2
   workup.STIRRINGThe mixture was stirred overnight
3. 3
   workup.ADDITIONwere added to the reaction mixture
4. 4
   workup.STIRRINGThe resulting mixture was shaken in a separatory funnel
5. 5
   기타the ethyl acetate layer was separated
6. 6
   세척washed with 0.5 M hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution
7. 7
   건조dried over anhydrous magnesium sulfate
8. 8
   여과filtered
9. 9
   농축concentrated under reduced pressure
10. 10
    기타The residue was purified by chromatography on a silica gel column

실험 절차

To a solution of 4-acetylthio-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)piperidine (400 mg, 1.27 mmol) (obtained as described in Reference Example 13) in dimethylformamide (12 ml) was added hydrazine acetate (152 mg, 1.65 mmol) at room temperature under an atmosphere of nitrogen and the mixture was stirred for 2.5 hours. After checking the completion of the reaction, a solution of p-nitrobenzyl (1R,5S,6S)-2-diphenylphosphoryloxy-6-[(R)-1-hydroxyethyl]-1-methylcarbapen-2-em-3-carboxylate (755 mg, 1.27 mmol) in acetonitrile (21 ml) was added dropwise to the resulting mixture in an ice bath under an atmosphere of nitrogen, followed by the addition of diisopropylethylamine (1.11 ml, 6.37 mmol). The mixture was stirred overnight while gradually raising the temperature to room temperature. After checking the completion of the reaction, ethyl acetate and saturated aqueous sodium hydrogencarbonate solution were added to the reaction mixture. The resulting mixture was shaken in a separatory funnel and the ethyl acetate layer was separated, washed with 0.5 M hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane: ethyl acetate (1:2) and ethyl acetate as the eluant to afford p-nitrobenzyl (1R,5S,6S)-2-[1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)piperidin-4-yl]thio-6-[(R)-1-hydroxyethyl]-1-methylcarbapen-2-em-3-carboxylate as a pale yellow solid (296 mg, yield 38%).

출처