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Lithium Hydroxide → TFA Cysteine 4-amino-3-methoxybenzoyl methionine

HRID 356084
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 356084
C([NH:8][C@H:9]([C:31]([OH:33])=[O:32])[CH2:10][S:11]C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)(OC(C)(C)C)=O.C[O:35][C:36](=[O:54])[C@H:37]([CH2:50][CH2:51][S:52][CH3:53])[NH:38][C:39](=[O:49])[C:40]1[CH:45]=[CH:44][C:43]([NH2:46])=[C:42]([O:47][CH3:48])[CH:41]=1.[Li+].[OH-].[SiH](CC)(CC)CC.[C:64]([OH:70])([C:66]([F:69])([F:68])[F:67])=[O:65].Cl.N[C@H](C(O)=O)CS.NC1C=CC(C(N[C@H](C(O)=O)CCSC)=O)=CC=1>C(Cl)Cl.O>[C:64]([OH:70])([C:66]([F:69])([F:68])[F:67])=[O:65].[NH2:8][C@H:9]([C:31]([OH:33])=[O:32])[CH2:10][SH:11].[NH2:46][C:43]1[CH:44]=[CH:45][C:40]([C:39]([NH:38][C@H:37]([C:36]([OH:54])=[O:35])[CH2:50][CH2:51][S:52][CH3:53])=[O:49])=[CH:41][C:42]=1[O:47][CH3:48]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 3939Lithium HydroxideHCID 6422Trifluoroacetic acidHCID 12052TriethylsilaneHCID 67601241N-BOC-S-trityl-cysteine 4-amino-3-methoxybenzoyl methionine methyl esterHCID 86753318HCl cysteine 4-aminobenzoyl methionine

Produkt 1

HCID 86753316
TFA Cysteine 4-amino-3-methoxybenzoyl methionine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel2×HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

N-BOC-S-trityl-cysteine-4-amino-3- methoxybenzoyl methionine methyl ester (0.18 g, 0.24 mmol) was deprotected with LiOH at room temperature as described above to give the free acid. The free acid was then further deprotected in CH2Cl2 (1.2 ml) with Et3SiH (0.04 ml, 0.24 mmol) and TFA (1.2 ml). The product was worked up as described for HCl-cysteine-4-aminobenzoyl methionine in Example 1, and HPLC revealed that the product was impure. The crude material was then purified on the HPLC using 0.1% TFA in water and acetonitrile as eluting solvents to result in two pure samples that were expected to be diastereomers. The major component (determined according to the major compound in the HPLC trace) was characterized as follows. mp sub 109° C., decomp 191°-193° C.; [α]25D =-30.0° (c=1, H2O), [α]25D =+19.0° (c=1, H2O); 1H NMR (CD3OD) 2.10 (3 H, s), 2.12-2.18 (1 H, m), 2.20-2.32 (1 H, m), 2.53-2.71 (2 H, m), 3.00 (1 H, dd, J=14.6, 7.5), 3.15 (1 H, dd, J=14.58, 4.8), 4.77 (1 H, dd, J=7.5, 4.8), 7.50 (1 H, d, J=8.4 Hz), 7.56 (1 H, s), 8.23 (1 H, d, J=8.4 Hz); 13C NMR (CD3OD) 15.20, 26.65, 31.60, 31.76, 53.27, 56.58, 56.76, 111.04, 121.08, 122.14, 130.85, 131.85, 150.88, 167.21, 169.61, 175.36; m/ z (FAB) for free amine, 402 (M+1).

Aufarbeitung

  1. customto give the free acid
  2. customThe crude material was then purified on the HPLC
  3. washas eluting solvents
  4. customto result in two pure samples that
  5. custommp sub 109° C., decomp 191°-193° C.

Quellen und Nachweise

ORD-Eintrag
ord-ad11bfc31e3a4c109302c524983929dc
Quelldatensatz
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05834434

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