(S)-(+)-3-Aminomethyl-5-methylhexanoic acid (pregabalin) was converted in one-pot to (S)-(-)-3-cyano-5-methylhexanoic acid (pregabalin nitrile) by N-dichlorination and double dehydrochlorination. The (S) β-cyanoacid was racemized under mild conditions by treatment with a base. This very simple and efficient procedure, applied to (R)-(-)-3-aminomethyl-5-methylhexanoic acid, would enable the recycling of the undesired enantiomer of pregabalin, an anticonvulsant drug manufactured by the synthesis of rac-3-aminomethyl-5- methylhexanoic acid and subsequent classical resolution.

From pregabalin to rac-3-cyano-5-methylhexanoic acid : an easy conversion which valorizes waste pregabalin enantiomer / M. Zagami, M. Binda, O. Piccolo, V. Straniero, E. Valoti, M. Pallavicini. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 53:45(2012 Nov 07), pp. 6075-6077. [10.1016/j.tetlet.2012.08.128]

From pregabalin to rac-3-cyano-5-methylhexanoic acid : an easy conversion which valorizes waste pregabalin enantiomer

M. Binda
Secondo
;
V. Straniero;E. Valoti
Penultimo
;
M. Pallavicini
Ultimo
2012

Abstract

(S)-(+)-3-Aminomethyl-5-methylhexanoic acid (pregabalin) was converted in one-pot to (S)-(-)-3-cyano-5-methylhexanoic acid (pregabalin nitrile) by N-dichlorination and double dehydrochlorination. The (S) β-cyanoacid was racemized under mild conditions by treatment with a base. This very simple and efficient procedure, applied to (R)-(-)-3-aminomethyl-5-methylhexanoic acid, would enable the recycling of the undesired enantiomer of pregabalin, an anticonvulsant drug manufactured by the synthesis of rac-3-aminomethyl-5- methylhexanoic acid and subsequent classical resolution.
Dichloroamine; Pregabalin; Pregabalin nitrile; Racemization; Trichloroisocyanuric acid
Settore CHIM/08 - Chimica Farmaceutica
7-nov-2012
Article (author)
File in questo prodotto:
File Dimensione Formato  
Tetrahedron Letters 53 (2012) 6075-772.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 267.23 kB
Formato Adobe PDF
267.23 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/213106
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 4
  • ???jsp.display-item.citation.isi??? 3
social impact