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Acetic Acid → 3-(4-thiazolyl)-L-alanine diphenylmethylester p-toluenesulfonate

HRID 429756
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 429756
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7]([OH:10])(=[O:9])=[O:8])=[CH:3][CH:2]=1.[S:12]1[CH:16]=[C:15]([CH2:17][C@@H:18]([C:20]([OH:22])=[O:21])[NH2:19])[N:14]=[CH:13]1.C1COCC1.[C:28]1([C:34]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)=[N+]=[N-])[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.C(O)(=O)C>C(O)C>[C:1]1([CH3:11])[CH:2]=[CH:3][C:4]([S:7]([OH:10])(=[O:8])=[O:9])=[CH:5][CH:6]=1.[C:28]1([CH:34]([O:21][C:20](=[O:22])[C@H:18]([CH2:17][C:15]2[N:14]=[CH:13][S:12][CH:16]=2)[NH2:19])[C:37]2[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=2)[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 176Acetic AcidHCID 8028TetrahydrofuranHCID 612301,1'-(Diazomethylene)bis(benzene)2×HCID 867576003-(4-thiazolyl)-L-alanine p-toluenesulfonate

Produkt 1

HCID 207060783-(4-thiazolyl)-L-alanine diphenylmethylester p-toluenesulfonateAusbeute 96,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

To a solution of 38.85 g of the compound (43) (112.8 mmol) in ethanol (200 ml)-THF (600 ml) was added diphenyldiazomethane (39 g, 201 mmol) little, by little over 30 min. at room temperature with stirring. After the reaction mixture was stirred for 1 h at room temperature, to the mixture was added diphenyldiazomethane (10 g, 51.5 mmol) and the resulting mixture was stirred for 1 h. To the reaction mixture was added acetic acid (0.1 ml) for quenching the excess reagent and the mixture was concentrated in vacuo. The residue (92 g) was crystallized by adding ether (1 L) to give 49.05 g (96.1%) of the compound (44).

Aufarbeitung

  1. stirringAfter the reaction mixture was stirred for 1 h at room temperature, to the mixture
  2. stirringthe resulting mixture was stirred for 1 h
  3. customfor quenching the excess reagent
  4. concentrationthe mixture was concentrated in vacuo
  5. customThe residue (92 g) was crystallized
  6. additionby adding ether (1 L)

Quellen und Nachweise

ORD-Eintrag
ord-c8878d1f1d7446cd84b6489225952cd9
Quelldatensatz
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06319902B1

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