Acetyl chloride → 8-(Pyridin-4-yl)-2,8-diazaspiro[4.5]decane dihydrochloride

HRID 1643448Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1643448
[N:1]1[CH:6]=[CH:5][C:4]([N:7]2[CH2:23][CH2:22][C:10]3([CH2:14][N:13](C(OC(C)(C)C)=O)[CH2:12][CH2:11]3)[CH2:9][CH2:8]2)=[CH:3][CH:2]=1.C([Cl:27])(=O)C>C(O)C>[ClH:27].[ClH:27].[N:1]1[CH:2]=[CH:3][C:4]([N:7]2[CH2:23][CH2:22][C:10]3([CH2:14][NH:13][CH2:12][CH2:11]3)[CH2:9][CH2:8]2)=[CH:5][CH:6]=1

Komponenten

4

Edukt 2

HCID 6367Acetyl chlorideHCID 59047377tert-Butyl 8-(pyridin-4-yl)-2,8-diazaspiro[4,5]decane-2-carboxylate

Produkt 1

HCID 667010648-(Pyridin-4-yl)-2,8-diazaspiro[4.5]decane dihydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

tert-Butyl 8-(pyridin-4-yl)-2,8-diazaspiro[4.5]decane-2-carboxylate (5.671 mmol, 1 eq) was dissolved in analytical grade ethanol (20 ml) and acetyl chloride (28.355 mmol, 3 eq.) was then added at 0° C. The mixture was stirred at 25° C. for 16 h. Thereafter, the solvent was concentrated in vacuo and the residue was dried under a high vacuum to obtain the desired product. Yield: 1.48 g (90%)

Aufarbeitung

  1. additionwas then added at 0° C
  2. concentrationThereafter, the solvent was concentrated in vacuo
  3. customthe residue was dried under a high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-c50502e521be4c7fa624a642f644a572
Quelldatensatz
uspto-grants-2012_02
Patentnummer
US08119805B2

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