<p><a href="https://www.lifechempharma.com/product/sodium-triacetoxyborohydride/">Sodium Triacetoxyborohydride </a></p>1-Boc-piperazine, also known as tert-butoxycarbonyl piperazine, is an organic compound widely used in organic synthesis, particularly as a protected form of piperazine. The term "Boc" stands for tert-butoxycarbonyl, a protecting group used to shield the nitrogen atom of piperazine during chemical reactions, making 1-Boc-piperazine a crucial intermediate in pharmaceuticals, fine chemicals, and peptide synthesis.Chemical Structure and Properties

Chemical Name: 1-Boc-piperazine
Molecular Formula: C₉H₁₈N₂O₂
Molecular Weight: 186.25 g/mol
CAS Number: 57260-71-6

Physical Properties:

The structure of 1-Boc-piperazine features a piperazine ring in which one nitrogen is protected by a tert-butoxycarbonyl group (-Boc), making it unreactive during certain reactions where the piperazine core is being modified.

1-Boc-piperazine is widely used as a key intermediate in chemical synthesis, particularly in:

Pharmaceuticals: The Boc group is used to protect the nitrogen atom in piperazine during multi-step organic synthesis. Piperazine derivatives are found in various drug classes, including antihistamines, antipsychotics, and anti-infective agents. The Boc-protected form enables selective reactions on other parts of the molecule without interfering with the piperazine ring.

Peptide Synthesis: In peptide chemistry, the Boc group is a common nitrogen-protecting group, which can be removed under acidic conditions (such as treatment with trifluoroacetic acid). This allows for selective deprotection, enabling controlled stepwise peptide bond formation.

Organic Synthesis: 1-Boc-piperazine is often employed in the synthesis of complex organic molecules. The presence of the Boc group protects the amine from reacting prematurely, allowing chemists to perform transformations elsewhere in the molecule.

1-Boc-piperazine is typically synthesized by reacting piperazine with di-tert-butyl dicarbonate (Boc₂O), which introduces the Boc protecting group onto one of the nitrogen atoms of the piperazine ring. The reaction occurs under mild conditions, typically in an organic solvent like dichloromethane or acetonitrile, and in the presence of a base such as triethylamine to neutralize the by-products.

The Boc protecting group is commonly used in organic chemistry due to its stability under basic and neutral conditions. It can be easily removed under acidic conditions, typically using trifluoroacetic acid (TFA) or hydrochloric acid, without affecting other functional groups. This feature makes Boc a versatile protecting group in complex multi-step syntheses.

Deprotection reaction: R-NH-Boc+TFA→R-NH2+CO2+tert-Butyl alcohol\text{R-NH-Boc} + \text{TFA} \rightarrow \text{R-NH}_2 + \text{CO}_2 + \text{tert-Butyl alcohol}R-NH-Boc+TFA→R-NH2​+CO2​+tert-Butyl alcohol

1-Boc-piperazine is considered relatively safe to handle under normal laboratory conditions. However, like all chemicals, it should be handled with appropriate personal protective equipment (PPE), including gloves, goggles, and lab coats. It is advisable to work with this compound in a well-ventilated area or under a fume hood, particularly during its synthesis or deprotection stages involving volatile acids such as TFA.

1-Boc-piperazine plays a critical role in medicinal chemistry. Piperazine derivatives are key structural motifs in a variety of therapeutic agents, including:

The Boc protection allows for selective modification and fine-tuning of the piperazine moiety in drug candidates, facilitating the development of new therapeutic agents.

1-Boc-piperazine is an indispensable reagent in organic and medicinal chemistry, particularly due to its role in protecting the piperazine nitrogen in complex synthetic processes. Its utility in pharmaceuticals, peptide synthesis, and organic transformations makes it a highly valuable compound, enabling precise and selective chemical modifications.