반응 #6002

반응 방정식

hydrochloride

nicotinoyl chloride

N-carbobenzoxydopamine

→

desired compound

수율 71.6%

3,4-di-O-nicotinoyl-N -carbobenzoxydopamine

수율 71.6%

용매

pyridine

반응 조건

후처리

1. 1
   기타to react at 35°-40° C. for 2 hours
2. 2
   workup.ADDITIONThen, the reaction mixture was poured into ice
3. 3
   추출a sodium carbonate solution followed by extraction with chloroform
4. 4
   추출The resulting extract
5. 5
   건조was dried over anhydrous magnesium sulfate
6. 6
   workup.DISTILLATIONthe solvent was distilled off
7. 7
   기타to obtain crude crystals
8. 8
   기타The thus-obtained crystals were recrystallized from ethyl acetate/diethyl ether (1:5 by volume)

실험 절차

19.0 g (66 mmol) of N-carbobenzoxydopamine obtained in Synthetic Example 1-(1) and 37.2 g (209 mmol) of hydrochloride of nicotinoyl chloride were added to 200 ml of pyridine. After stirring at room temperature for 12 hours, the mixture was allowed to react at 35°-40° C. for 2 hours. Then, the reaction mixture was poured into ice and a sodium carbonate solution followed by extraction with chloroform. The resulting extract was dried over anhydrous magnesium sulfate and the solvent was distilled off to obtain crude crystals. The thus-obtained crystals were recrystallized from ethyl acetate/diethyl ether (1:5 by volume) to obtain 23.5 g (yield: 71.6%) of the desired compound in the form of white crystals (m.p. 77°-78° C.).

출처