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
N—BOC—O-allyl-tyrosine (obtained from NeoMPS, San Diego, Calif. 92126, USA) (10.0 g, 32.5 mmol), HATU (12.4 g, 35.8 mmol) and leucine methyl ester hydrochloride (5.90 g, 65.0 mmol) were dissolved in anhydrous DMF (50 mL). DIPEA (22.7 mL, 130 mmol) was added and the reaction mixture was stirred at rt for 18 h before being partitioned between EtOAc and 1M hydrochloric acid. The organic phase was then washed sequentially with 1M hydrochloric acid and brine before being dried (MgSO4), filtered and concentrated in vacuo. Purification was achieved using flash chromatography, eluting with a gradient of 1/5 EtOAc/(50/70) petroleum ether to 100% EtOAc to yield a white solid, 8.45 g, 58%. Rf=0.33 (1/3 EtOAc/(50/70) petroleum ether).
WORKUP
后处理
- custombefore being partitioned between EtOAc and 1M hydrochloric acid
- washThe organic phase was then washed sequentially with 1M hydrochloric acid and brine
- dry with materialbefore being dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customPurification
- washeluting with a gradient of 1/5 EtOAc/(50/70) petroleum ether to 100% EtOAc
- customto yield a white solid, 8.45 g, 58%