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

HRID 1383722
ノート
印刷プレビュー

反応式

HRID 1383722 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 5

HCID 142844-(Dimethylamino)pyridine触媒
HCID 6228
Dimethylformamide
溶媒
HCID 6344Dichloromethane溶媒
HCID 6422Trifluoroacetic acid溶媒2 回
HCID 8857Ethyl Acetate溶媒

実験手順

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%).

後処理

  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)

出典と根拠

ORDレコード
ord-c8c41c1ee69e4625a1b4a44dacda4158
出典データセット
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06255285B1

反応ノート

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