Z-Gln-ONp → H-Gln-Thr-Pro-OtBu
반응식
[NH2:1][C@H:2]([C:6]([N:8]1[CH2:19][CH2:18][CH2:17][C@H:9]1[C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[O:7])[C@@H:3]([CH3:5])[OH:4].C1C=CC(COC([NH:30][C@H:31]([C:37](OC2C=CC([N+]([O-])=O)=CC=2)=[O:38])[CH2:32][CH2:33][C:34]([NH2:36])=[O:35])=O)=CC=1>CN(C=O)C>[NH2:30][C@H:31]([C:37]([NH:1][C@H:2]([C:6]([N:8]1[CH2:19][CH2:18][CH2:17][C@H:9]1[C:10]([O:12][C:13]([CH3:15])([CH3:14])[CH3:16])=[O:11])=[O:7])[C@@H:3]([CH3:5])[OH:4])=[O:38])[CH2:32][CH2:33][C:34](=[O:35])[NH2:36]참가 물질
4
실험 절차
1.36 g H-Thr-Pro-OtBu is dissolved in 10 ml DMF, after which 1.93 g Z-Gln-ONp is added and the reaction mixture is stirred for about 20 hours at room temperature. After evaporation of the mixture to dryness, the residue is dissolved in EtOAc and washed consecutively with 5% KHSO4 solution, 5% NaHCO3 solution and a saturated NaCl solution. The solution is then dried over Na2SO4 and filtered, and the filtrate is evaporated to dryness.
후처리
- customAfter evaporation of the mixture to dryness
- dissolutionthe residue is dissolved in EtOAc
- washwashed consecutively with 5% KHSO4 solution, 5% NaHCO3 solution
- dry with materialThe solution is then dried over Na2SO4
- filtrationfiltered
- customthe filtrate is evaporated to dryness
출처 및 근거
- ORD 기록
- ord-b22a67e408404ba19122d28e54dd56bc
- 출처 데이터셋
- uspto-grants-1981_06
- 특허 번호
- US04271152
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