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The author is not a physician. The content on this website does not, and is not intended to constitute medical advice. It should not be relied upon when making medical decisions. It is not intended as a substitute for advice from your physician or other healthcare provider.

« Chirality Matters... | Main | Propidium Iodide (A rare derivative) »

Tetrazole (Weird acids)

Category: Synthesis
Posted on: June 16, 2008 10:39 PM, by Molecule of the Day

That was probably the longest break ever. I'm trying to do better, but writing up multiple papers and grant applications, along with a pretty intense summer travel schedule just haven't augured well for the blogging. Onward and upward: tetrazole.


Tetrazole is one of those molecules I didn't believe existed off paper the first time I saw it. Lots of electronegative atoms in a row (usually nitrogens and oxygens) typically indicates something unstable, if not explosive, but aromaticity does its work here, and tetrazole works well. So well, in fact, that it works in that mild-as-mothers-milk environment of biomolecular synthesis. It will protonate a DNA monomer, thus activating it for solid-phase synthesis.

Comments

It also has the interesting property of being quite acidic (pKa 4.89). It is often used as a bioisosteric replacement for a carboxylic acid in medicinal chemistry. Often better bioavailability than the carboxylic acid.
Cool synthesis via cycloaddition of azide with a nitrile and you have your substitutet tetrazole of choice.

Posted by: Nanono | June 17, 2008 8:25 AM

Reduce tetrazole's carbon footprint (17.15 wt-% C) as tetrazole azide (10.81 wt-% C) and sell the carbon credits. Isn't that what Enviro-whinerism is all about? Couple the anion with iodine to get a chain of eight nitrogens. That ought to do something.

Posted by: Uncle Al | June 17, 2008 11:46 AM

It is pretty expensive, oligo-people at the institute in Prague where I used to work were making it by diazotation and H3PO2-reduction of diazonium made from 5-aminotetrazole (much cheaper). They shared few grams with me which I had to purify for my own work by sublimation. You have to heat it quite high, close to the melting point -which made me rather nervous - but the sublimation it went without accident.

A great reagent for fosphoramidite method of phosphorylating serine, threonine in peptides, under mild conditions - it works there as acid catalyst and its anion like a supernucleophile, think of acidic DMAP

Posted by: milkshake | June 17, 2008 10:00 PM

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