(2-((Tert-butoxycarbonyl)amino)pyridin-4-yl)boronic acid

Name: (2-((Tert-butoxycarbonyl)amino)pyridin-4-yl)boronic acid
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CAS No. 903513-59-7
Cat. No. CS-0573703
Purity≥98%
MDL No.MFCD13188969

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(2-((Tert-butoxycarbonyl)amino)pyridin-4-yl)boronic acid|CS-0573703

Structure of 903513-59-7

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General Information

CAS No. 903513-59-7
Cat. No. CS-0573703
Purity ≥98%
MDL No. MFCD13188969
Storage -20°C, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₀H₁₅BN₂O₄
Molecular Weight 238.05
Synonym(s) 2-(tert-butoxycarbonylamino)pyridin-4-ylboronic acid
SMILES B(C1=CC(=NC=C1)NC(=O)OC(C)(C)C)(O)O

Description

This boronate moiety integrates a tert-butoxycarbonyl-protected pyridyl amine, enabling stable, orthogonal functionalization in late-stage diversification. The electron-deficient pyridine ring enhances reactivity in cross-coupling processes while the Boc group provides robust protection under standard conditions.

Application

(2-((Tert-butoxycarbonyl)amino)pyridin-4-yl)boronic acid serves as a versatile building block for constructing pyridine-based heterocycles and bioactive molecules. Its boronic acid functionality enables efficient Suzuki-Miyaura coupling under standard conditions, while the Boc-protected amine offers orthogonal reactivity and enhanced stability during synthesis. The compound exhibits excellent bench stability, simplifies purification, and is compatible with diverse functional groups, making it ideal for medicinal chemistry and process development workflows.

Safety Information

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Computational Chemistry Data

TPSA 91.68
LogP 0.1084
H_Acceptors 5
H_Donors 3
Rotatable_Bonds 2

Other Classifications

Building Blocks Functional Group Boronic Acid And Its Ester

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Key Words

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(2-((Tert-butoxycarbonyl)amino)pyridin-4-yl)boronic acid

CAS No. 903513-59-7

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