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Z-Phe-ONp → Z-Phe-Val-N-Me-Tyr(3-tBu)-NH2

HRID 1383722
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HRID 1383722 반응식
[NH:1](C(OC(C)(C)C)=O)[C@H:2]([C:6]([N:8]([CH3:25])[C@H:9]([C:22]([NH2:24])=[O:23])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([C:18]([CH3:21])([CH3:20])[CH3:19])[CH:12]=1)=[O:7])[CH:3]([CH3:5])[CH3:4].N[C@H](C(N(C)[C@H](C(N)=O)CC1C=CC(O)=C(C(C)(C)C)C=1)=O)C(C)C.[CH:58]1[CH:63]=[CH:62][C:61]([CH2:64][C@H:65]([NH:78][C:79]([O:81][CH2:82][C:83]2[CH:88]=[CH:87][CH:86]=[CH:85][CH:84]=2)=[O:80])[C:66](OC2C=CC([N+]([O-])=O)=CC=2)=[O:67])=[CH:60][CH:59]=1>C(Cl)Cl.C(O)(C(F)(F)F)=O.CN(C=O)C.CN(C1C=CN=CC=1)C.C(OCC)(=O)C>[NH:78]([C:79]([O:81][CH2:82][C:83]1[CH:88]=[CH:87][CH:86]=[CH:85][CH:84]=1)=[O:80])[C@H:65]([C:66]([NH:1][C@H:2]([C:6]([N:8]([CH3:25])[C@H:9]([C:22]([NH2:24])=[O:23])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([C:18]([CH3:21])([CH3:19])[CH3:20])[CH:12]=1)=[O:7])[CH:3]([CH3:5])[CH3:4])=[O:67])[CH2:64][C:61]1[CH:60]=[CH:59][CH:58]=[CH:63][CH:62]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 3

HCID 151025Z-Phe-ONpHCID 131722737Boc-Val-N-Me-Tyr(3-tBu)-NH2HCID 131722740Val-N-Me-Tyr(3-tBu)-NH2

생성물 1

HCID 131722739Z-Phe-Val-N-Me-Tyr(3-tBu)-NH2

시약·촉매·용매 5

HCID 142844-(Dimethylamino)pyridine촉매
HCID 6228
Dimethylformamide
용매
HCID 6344Dichloromethane용매
HCID 6422Trifluoroacetic acid용매2회
HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 146 mg (0.325 mmol) of Boc-Val-N-Me-Tyr(3-tBu)-NH2 in 2 ml of methylene chloride, 1 ml of TFA was added and the mixture was stirred at room temperature for 30 minutes. The solvent was distilled off under reduced pressure. To a solution of the resulting TFA salt of Val-N-Me-Tyr(3-tBu)-NH2 in 2 ml of DMF, 0.1 ml of TEA, 219 mg (0.348 mmol) of Z-Phe-ONp and 93.5 mg (0.765 mmol) of DMAP were added and the mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with ethyl acetate and washed first with saturated aqueous NaHCO3, then with water and finally with saturated brine. The organic layer was dried with anhydrous magnesium sulfate and concentrated under reduced pressure; the resulting residue was subjected to silica gel column chromatography (eluting solvent; ethyl acetate:n-hexane=1:1) to give Z-Phe-Val-N-Me-Tyr(3-tBu)-NH2 in the amount of 189 mg (92%).

후처리

  1. distillationThe solvent was distilled off under reduced pressure
  2. stirringthe mixture was stirred at room temperature for 2 hours
  3. washwashed first with saturated aqueous NaHCO3
  4. dry with materialThe organic layer was dried with anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. washthe resulting residue was subjected to silica gel column chromatography (eluting solvent; ethyl acetate:n-hexane=1:1)

출처 및 근거

ORD 기록
ord-c8c41c1ee69e4625a1b4a44dacda4158
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06255285B1

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