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Topic: Question about amidation  (Read 2211 times)

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Offline Harold.Han

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Question about amidation
« on: June 28, 2010, 05:16:26 PM »
I want to have a very simple reaction between -NH2 and methyl ester in MeOH.

Because the compound containing Methyl ester has sugar rings and double bonds, I can not do an intensive reaction.

What I really want to do is put Et3N in the system and react at RT.

Can somebody tell me whether it will work?

Thanks!


Offline OC pro

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Re: Question about amidation
« Reply #1 on: June 29, 2010, 03:14:26 PM »
It will react extremely slowly. More better is to convert the ester to acid. Then you can use standard peptide coupling reagents (e.g. EDC, TBTU and so on).

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