PyAOP reagent

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PyAOP reagent
PyAOP Structure.svg
Names
IUPAC name
(7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate
Other names
PyAOP
Identifiers
3D model (JSmol)
ChemSpider
UNII
Properties
C17H27F6N7OP2
Molar mass 521.389 g·mol−1
Appearance White crystals
Melting point 163–168 °C (325–334 °F; 436–441 K)
Hazards
Main hazards Irritant
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

PyAOP ((7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate) is a coupling reagent used in solid phase peptide synthesis. It is a derivative of the HOAt family of coupling reagents. It is preferred over HATU, because it does not side react at the N-terminus of the peptide.[1] Compared to the HOBt derivates, PyAOP (and HOAt in general) are more reactive due to the additional nitrogen.[2]

See also

References

  1. Albericio, F.; Cases, M.; Alsina, J.; Triolo, S. A.; Carpino, L. A; Kates, S. (1997). "On the use of PyAOP, a phosphonium salt derived from HOAt, in solid-phase peptide synthesis". Tetrahedron Letters 38 (27): 4853–4856. doi:10.1016/S0040-4039(97)01011-3. 
  2. Albericio, Fernando; Bofill, Josep M.; El-Faham, Ayman; Kates, Steven A. (1998). "Use of Onium Salt-Based Coupling Reagents in Peptide Synthesis1". The Journal of Organic Chemistry (American Chemical Society) 63 (26): 9678–9683. doi:10.1021/jo980807y. ISSN 0022-3263. 




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