L-Tyrosine ethyl ester → HCID 12136556, 화합물
반응식
[NH2:1][C@H:2]([C:11]([O:13]CC)=O)[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.[NH2:16][C@H:17]([C:22]([O:24]CC)=[O:23])[CH2:18][CH2:19][CH2:20][NH2:21].Cl.Cl>>[NH2:1][C@H:2]([C:11]([NH:16][C@H:17]([C:22]([OH:24])=[O:23])[CH2:18][CH2:19][CH2:20][NH2:21])=[O:13])[CH2:3][C:4]1[CH:5]=[CH:6][C:7]([OH:10])=[CH:8][CH:9]=1참가 물질
3
실험 절차
It is also possible according to the present invention to employ a non-proteinogenic amino acid as a nucleophile. Mal-Tyr-OEt, an electrophile, and Orn-OEt.2HCl, a nucleophile, were reacted using α-CT as a catalyst. After a reaction time of 20 minutes, the solution was concentrated, the enzyme was separated off by ultrafiltration with a membrane with MWCO 10,000, and the dissolved fraction was lyophilized. Both Mal-Tyr-Orn and the Orn delta-lactam cyclization product were isolated by preparative HPLC and identified by 1H-NMR. The combined yield of the two products (about 1:1) was about 45-50%.
후처리
- concentrationAfter a reaction time of 20 minutes, the solution was concentrated
- customthe enzyme was separated off by ultrafiltration with a membrane with MWCO 10,000