Propose a mechanism for the rearrangement of the thiazoline obtained from the reaction of Edman's reagent with a peptide to a PTH-amino acid. (Hint: Thioesters are very reactive toward nucleophiles.)

Verified step by step guidance

1. Identify the starting material: The thiazoline is formed from the reaction of Edman’s reagent (phenyl isothiocyanate, Ph-N=C=S) with the N-terminal amino group of the peptide. This forms a cyclic intermediate known as thiazoline.
2. Recognize the reactivity of thioesters: Thioesters are highly reactive toward nucleophiles due to the poor overlap between the sulfur atom's orbitals and the carbonyl carbon, making the carbonyl carbon more electrophilic.
3. Propose the nucleophilic attack: A water molecule (acting as a nucleophile) attacks the electrophilic carbonyl carbon of the thioester in the thiazoline ring. This leads to the opening of the thiazoline ring and the formation of a tetrahedral intermediate.
4. Facilitate the rearrangement: The tetrahedral intermediate collapses, expelling the sulfur-containing group and forming a new carbonyl group. This results in the formation of the phenylthiohydantoin (PTH) derivative of the amino acid.
5. Conclude the mechanism: The final product is the PTH-amino acid, which is stable and can be identified to determine the N-terminal amino acid of the peptide.

Key Concepts

Thiazoline Chemistry

Thiazolines are five-membered heterocycles containing both sulfur and nitrogen. In the context of Edman's reagent, thiazolines are formed when the reagent reacts with the amino group of a peptide. Understanding the structure and reactivity of thiazolines is crucial for proposing a rearrangement mechanism, as their unique properties influence how they interact with other molecules.

PTH-Amino Acid Formation

Phenylthiohydantoin (PTH) amino acids are derivatives formed during the Edman degradation process, which is used for sequencing peptides. The conversion of thiazoline to PTH-amino acids involves a series of nucleophilic attacks and rearrangements. Recognizing the steps involved in this transformation is essential for accurately proposing the mechanism of rearrangement.

Reactivity of Thioesters

Thioesters are highly reactive compounds that can undergo nucleophilic attack due to the electrophilic nature of the carbonyl carbon. In the context of the rearrangement mechanism, the hint suggests that thioesters formed during the reaction can react with nucleophiles, facilitating the conversion of thiazoline to PTH-amino acids. Understanding this reactivity is key to predicting the pathway of the rearrangement.