反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of tert-butyl (2-oxoethyl)carbamate (1 eq; 0.38 M) in dry MeOH was added a mixture of methyl (7R)-14-cyclohexyl-7-(methylamino)-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate(0.14 M), acetic acid (2 eq) and sodium acetate (1 eq) in dry MeOH, and the mixture stirred at RT for 15 min. Then Pd/C (0.3 weight eq) was added as a slurry in MeOH under N2. The atmosphere in the reaction vessel was charged with H2, and the reaction stirred vigorously under a H2 atmosphere (balloon) at 60° C. overnight. The reaction was allowed to cool to RT, flushed with N2 and filtered through a plug of CELITE. The filtrate was concentrated in vacuo and the residue purified by FC (PE/EtOAc 2.5:1 to 1.5:1 gradient) to afford the title compound (82%). (ES+) m/z 562 (M+H)+; [α]D +67.1, c=0.67, CHC13
WORKUP
后处理
- additionThe atmosphere in the reaction vessel was charged with H2
- stirringthe reaction stirred vigorously under a H2 atmosphere (balloon) at 60° C. overnight
- temperatureto cool to RT
- customflushed with N2
- filtrationfiltered through a plug of CELITE
- concentrationThe filtrate was concentrated in vacuo
- customthe residue purified by FC (PE/EtOAc 2.5:1 to 1.5:1 gradient)