تفاعل #43417

معادلة التفاعل

[3,8-difluoro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl]methyl 4-methylbenzenesulfonate

sodium carbonate

1,1-dimethylethyl 4-piperidinylcarbamate

→

1,1-dimethylethyl (1-{[3,8-difluoro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl]methyl}-4-piperidinyl)carbamate

المذيبات

ethanol

ظروف التفاعل

المعالجة

1. 1
   أخرىevaporated
2. 2
   workup.ADDITIONtreated with water (200 mL)
3. 3
   استخلاصThe aqueous layer was extracted with a 10% solution of methanol in dichloromethane (3×200 mL)
4. 4
   تجفيفthe combined organic extracts dried over magnesium sulphate
5. 5
   أخرىevaporated
6. 6
   أخرىThe residue was chromatographed
7. 7
   غسيلeluting with a 0-10% gradient of methanol in dichloromethane affording a yellow solid (1.1 g, 91%)

الإجراء التجريبي

A solution of crude [3,8-difluoro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl]methyl 4-methylbenzenesulfonate (1.2 g, 2.79 mmol) in ethanol (40 mL) was treated with sodium carbonate (889 mg, 8.38 mmol) and 1,1-dimethylethyl 4-piperidinylcarbamate (615 mg, 3.07 mmol). The reaction mixture was stirred at room temperature for 18 hours under argon, evaporated and treated with water (200 mL). The aqueous layer was extracted with a 10% solution of methanol in dichloromethane (3×200 mL) and the combined organic extracts dried over magnesium sulphate and evaporated. The residue was chromatographed eluting with a 0-10% gradient of methanol in dichloromethane affording a yellow solid (1.1 g, 91%).

المصدر