反应详情

A suspension of 172.5 g (0.75 mol) of 6-(4-aminophenyl)-1,2-dihydro-2-oxonicotinic acid, 312 ml (2.23 mol) of triethylamine, and 11.8 L of dichloromethane is stirred at 10° and 290 ml (2.28 mol) of chlorotrimethylsilane is slowly added. The resulting mixture is stirred overnight at room temperature. A mixture of 273 g (1.58 mol) of N-acetyl-4-hydroxy-L-proline and 3.5 L of dichloromethane is stirred at -15° and 177.5 ml (1.61 mol) of N-methylmorpholine is added during a 20 min period followed by 250 ml of dichloromethane as a wash. The mixture is stirred at -13° for 15 min and 125.5 ml (1.62 mol) of methyl chloroformate is added over a 25 min period at -14° followed by 150 ml of dichloromethane as a wash. The mixture is stirred at -15° for 40 min and the above silylated nicotinic acid is added over a period of 60 min at -17° followed by 500 ml of dichloromethane as a rinse. The mixture is stirred for 1 hr and 40 min as the temperature rose to 1°. The mixture is stirred overnight with ice bath cooling as the temperature rose to 16° and 135 ml of glacial acetic acid is added followed by 135 ml of isopropanol. The reaction mixture is concentrated to 4 L under reduced pressure and the solid filtered, washed with dichloromethane and dried to give 245 g of 6-[4-(N-acetyl-4-hydroxy-L-prolylamino)phenyl]-1,2-dihydro-2-oxonicotinic acid.

1. stirringThe resulting mixture is stirred overnight at room temperature
2. stirringis stirred at -15°
3. stirringThe mixture is stirred at -13° for 15 min
4. stirringThe mixture is stirred at -15° for 40 min
5. stirringThe mixture is stirred for 1 hr and 40 min as the temperature
6. customrose to 1°
7. stirringThe mixture is stirred overnight with ice bath
8. temperaturecooling as the temperature
9. customrose to 16°
10. concentrationThe reaction mixture is concentrated to 4 L under reduced pressure
11. filtrationthe solid filtered
12. washwashed with dichloromethane
13. customdried