Pyridine → 3,4-di-O-isobutyryl-N-carbobenzoxydopamine

反応式

[C:1]([NH:11][CH2:12][CH2:13][C:14]1[CH:21]=[CH:20][C:18]([OH:19])=[C:16]([OH:17])[CH:15]=1)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].[C:22](Cl)(=[O:26])[CH:23]([CH3:25])[CH3:24].[C:28](=[O:31])([O-])[O-].[Na+].[Na+].N1C=C[CH:37]=[CH:36][CH:35]=1>>[C:22]([O:17][C:16]1[CH:15]=[C:14]([CH:21]=[CH:20][C:18]=1[O:19][C:28](=[O:31])[CH:36]([CH3:37])[CH3:35])[CH2:13][CH2:12][NH:11][C:1]([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:2])(=[O:26])[CH:23]([CH3:25])[CH3:24]

参加物

反応物 4

HCID 1049Pyridine

HCID 10340Sodium Carbonate

HCID 62325Isobutyryl chloride

HCID 11108946Benzyl N-[2-(3,4-dihydroxyphenyl)ethyl]carbamate

生成物 1

HCID 1317181703,4-di-O-isobutyryl-N-carbobenzoxydopamine収率 74.7%

実験手順

To 80 ml of a pyridine solution containing 10.7 g (37 mmol) of N-carbobenzoxydopamine obtained in Synthetic Example 1-(1) was added dropwise 9.9 g (93 mmol) of isobutyryl chloride at 5° to 10° C. After stirring at room temperature for 12 hours, the mixture was allowed to react at 35° to 40° C. for 3 hours. Then, the reaction mixture was poured into ice and a sodium carbonate solution and stirred at room temperature for 30 minutes. The mixture was extracted with diethyl ether and the resulting extract was dried over anhydrous magnesium sulfate. The solvent was distilled and the thus-obtained crude crystals were recrystallized from diisopropyl ether/petroleum ether (1:2 by volume) to obtain 11.9 g (yield: 74.7%) of the desired compound in the form of white cyrstals (m.p. 44°-46° C.).