Hydrochloric Acid → 5-(3-Amino-propyl)-thiophene-2-carboxylic acid tert-butyl ester hydrochloride

HRID 1699073Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1699073
[C:1]([O:5][C:6]([C:8]1[S:9][C:10]([C:13]#[C:14][CH2:15][NH:16]C(OCC2C=CC=CC=2)=O)=[CH:11][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[ClH:27]>CO.[OH-].[OH-].[Pd+2]>[ClH:27].[C:1]([O:5][C:6]([C:8]1[S:9][C:10]([CH2:13][CH2:14][CH2:15][NH2:16])=[CH:11][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Komponenten

5

Edukt 2

HCID 313Hydrochloric AcidHCID 545289645-(3-Benzyloxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic acid tert-butyl ester

Produkt 1

HCID 695442585-(3-Amino-propyl)-thiophene-2-carboxylic acid tert-butyl ester hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 9942167Palladium hydroxideKatalysatorHCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 5-(3-benzyloxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic acid tert-butyl ester (1.0 g, 2.69 mmol) in 15 mL MeOH and 2.69 mL 1N HCl (aq) was added Pd(OH)2 (1 g). The mixture was shaken in a Parr shaker under 45 psi H2 for 16 h. The catalyst was removed by filtration through Celite and additional Pd(OH)2 (1 g) was added. The reaction was shaken at 45 psi H2 for 6 h and the catalyst was removed by filtration through Celite. The solution was concentrated in vacuo. The residue was azeotroped with CCl4 and was triturated with Et2O to provide the title amine (360 mg).

Aufarbeitung

  1. customThe catalyst was removed by filtration through Celite and additional Pd(OH)2 (1 g)
  2. additionwas added
  3. stirringThe reaction was shaken at 45 psi H2 for 6 h
  4. customthe catalyst was removed by filtration through Celite
  5. concentrationThe solution was concentrated in vacuo
  6. customThe residue was azeotroped with CCl4
  7. customwas triturated with Et2O

Quellen und Nachweise

ORD-Eintrag
ord-4a5c264e90d44ea893c55e07350e4373
Quelldatensatz
uspto-grants-2002_02
Patentnummer
US06344485B1

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