摘要
在固相多肽合成中,探索一种经济有效的Boc保护氨基酸键合氯甲基树脂的方法.采用K_2CO_3/KI作为键合试剂,一步合成产物,反应条件为:Boc保护氨基酸2.5倍量,K_2CO_32.5倍量,KI0.01倍量,氯甲基树脂1.0倍量,普通DMF作反应溶剂,70℃空气浴中旋转反应25h.考察了28种不同结构的氨基酸底物在此条件下与氯甲基树脂的键合收率,大多数氨基酸都能得到几乎定量的酯化产率.并选取了不同空间位阻的4种Boc保护氨基酸,比较了KOH,Cs_2CO_3,TEA/KI,DCHA/KI,DIPA/KI,Cs_2CO_3/KI和K_2CO_3/KI等不同键合条件对收率的影响.结果表明,除Boc-Asn-OH外,K_2CO_3/KI条件与Cs_2CO_3/KI的效果大体相同,但K_2CO_3/KI更为经济、可行.
An efficient and economical technology for the anchoring of Boc-protected amino acids via the carboxy terminal to chloromethyl Merrifield resin, using K2CO3/KI as the base reagent, was investigated. 2.5 equiv. Boc-AA-OH, 2.5 equiv. K2CO3, 0.01 equiv. KI and 1.0 equiv, resin were mixed in DMF. The reaction was completed after 25 h at 70℃. Each of the twenty-eight N-blocked amino acids was attached to Merrifield chloromethyl resin to give the N-Boc-esterified resin preparations. The mean values of yields were based on both weight gain of the resin and the nitrogen content respectively. Most yields of the desired deri- vatized resin esters were close to quantitative level. Four amino acids with different bulk of side chain were compared in the resin loading experiment under seven different conditions, such as KOH, Cs2CO3, TEA/KI, DCHA/KI, DIPA/KI, Cs2CO3/KI and K2CO3/KI. The efficiency of K2CO3/KI in related reaction was the same as that of Cs2CO3/KI, except for Boc-Asn-OH. Considering the facility and economy, K2CO3/KI promoted process would be more suitable for large scale production of chloromethyl resin bound Boc-amino acids.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2007年第4期536-540,共5页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No.30572244)资助项目.