Diphenylphosphoryl Azide (DPPA) - A Reagent with Manifold Applications

Biographical Sketches

Huan Liang was born in Tianjin, P. R. of China in 1980. He received his B.Sc. in Chemistry from Tianjin University in 2003. He is now pursuing his Ph.D. under the supervision of Prof. Marco Ciufolini, Canada Research Chair in Synthetic Organic Chemistry, at the University of British Columbia. His research mainly focuses on natural product synthesis for pharmaceutical application.

Introduction

Diphenylphosphoryl azide, originally developed by Yamada­ in 1972, [¹] has shown significant synthetic versatility, [²] being used in isocyanate synthesis, especially in the Curtius rearrangement, [¹] stereospecific conversion of alcohol into azide, [³] as a coupling reagent in macrolactamization, [4] in allylic amine synthesis, [5] and in aziridination reactions. [6]

Diphenylphosphoryl azide, also called DPPA, diphenyl phosphorazidate or phosphoric acid diphenyl ester azide, is a colorless liquid with high boiling point (157 ˚C/0.17 mmHg), and can be easily prepared by the reaction between diphenylphosphoryl chloride and sodium azide in acetone in high yield. [¹] [7] The Waldvogel group developed a reliable protocol for the large-scale (100 g) synthesis of DPPA, including purification by reduced-pressure distillation (Scheme  [¹] ). [8] A polymer-supported form of the reagent has also been developed using phenol resin by the Taylor group. [9]

Scheme 1 Preparation of DPPA in 400 mmol scale

Abstracts

(A) Yamada and co-workers developed an improved method for the Curtius rearrangement reaction using DPPA, which was later named Yamada-Curtius rearrangement. [¹] In 2007, the Ciufolini group employed this method in the total synthesis of streptonigrone, to transform a carboxylic acid group into a protected amino group through the hydrolysis of an isocyanate intermediate. [¹0]
(B) A primary or secondary alcohol can be easily converted into an azide group by DPPA under mildly basic conditions or using Mitsunobu­ conditions for stereochemical inversion. In the total synthesis of cribrostatin VI, the Danishefsky group successfully employed DPPA to displace a benzyl alcohol in high yield and ee. [¹¹] Another example was demonstrated in the synthesis of Tamiflu and its phosphonate congeners by the Wang group in 2007. [¹²]
(C) Diphenylphosphoryl azide has also been widely used in peptide coupling reactions, particularly in macrolactamization. [4] In 2005, the Moody group completed the synthesis of thiopeptide amythiamicin D. In the final step, after global deprotection of N-Boc and tert-butyl groups, an α-amino ketone was successfully coupled with a thiazole carboxylic acid in DMF in 73% yield. [¹³]
(D) The Batey group has developed a stereoselective synthesis of allylic amines through a [3,3]-aza-phospha-oxa-Cope sigmatropic rearrangement. [5] Methylvinylcarbinol was converted into crotylamine in 85% yield over two steps. DPPA was used as an amine source in these reactions, and excellent selectivity was achieved through addition of a catalytic amount of PdCl2(MeCN)2 catalyst.
(E) A new catalytic aziridination reaction using cobalt tetraphenyl­porphyrin [Co(TPP)] as catalyst has been extensively studied by the Zhang group. [6] DPPA functioned as a nitrene source in the reaction that proceeded in good to excellent yield.

References

• 1a Shioiri T. Ninomiya K. Yamada S. J. Am. Chem. Soc.  1972,  94:  6203 
• 1b Ninomiya K. Shioiri T. Yamada S. Tetrahedron  1974,  30:  2151 
• 2 Bräse S. Gil C. Knepper K. Zimmermann V. Angew. Chem. Int. Ed.  2005,  44:  5188 
• 3a Thompson AS. Humphrey GR. DeMarco AM. Mathre DJ. Grabowski EJJ. J. Org. Chem.  1993,  58:  5886 
• 3b Hughes DL. Org. React.  1992,  42:  335 
• 4 Han SY. Kim YA. Tetrahedron  2004,  60:  2447 
• 5a Lee EE. Batey RA. Angew. Chem. Int. Ed.  2004,  43:  1865 ; Angew. Chem. 2004, 116, 1901
• 5b Lee EE. Batey RA. J. Am. Chem. Soc.  2005,  127:  14887 
• 6 Gao GY. Jones JE. Vyas R. Harden JD. Zhang XP. J. Org. Chem.  2006,  71:  6655 
• 8 Wolff O. Waldvogel SR. Synthesis  2004,  1303 
• 9 Lu Y. Taylor RT. Tetrahedron Lett.  2003,  44:  9267 
• 10 Chan BK. Ciufolini MA. J. Org. Chem.  2007,  72:  8489 
• 11 Chan C. Heid R. Zheng S. Guo J. Zhou B. Furuuchi T. Danishefsky SJ. J. Am. Chem. Soc.  2005,  127:  4596 
• 12 Shie JJ. Fang JM. Wang SY. Tsai KC. Cheng YSE. Yang AS. Hsiao SC. Su CY. Wong CH. J. Am. Chem. Soc.  2007,  129:  11892 
• 13 Hughes RA. Thompson SP. Alcaraz L. Moody CJ. J. Am. Chem. Soc.  2005,  127:  15644 

7

Appropriate safety measures are necessary when using DPPA, a source of toxic azide ion. (LD₅₀ of azide ion 29 mg/kg in rats, calculated from LD₅₀ of NaN₃ as per Merck index). Also, like all organic azides, DPPA should be regarded as potentially explosive.