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tert-Butyl ((2-bromopyridin-4-yl)methyl)carbamate

  • CAS No. 1049025-21-9

  • Cat. No. CS-0059178
  • Purity≥98%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

tert-Butyl ((2-bromopyridin-4-yl)methyl)carbamate|CS-0059178

Structure of 1049025-21-9

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General Information

  • CAS No. 1049025-21-9
  • Cat. No. CS-0059178
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₅BrN₂O₂
  • Molecular Weight 287.15
  • Synonym(s) 4-(N-Boc-aminomethyl)-2-bromopyridine
  • SMILES O=C(OC(C)(C)C)NCC1=CC(Br)=NC=C1

Description

tert-Butyl ((2-bromopyridin-4-yl)methyl)carbamate delivers a brominated pyridylmethyl scaffold with orthogonal protection, enabling direct functionalization at the pyridine ring. The carbamate group ensures stability during storage and facilitates selective deprotection under mild acidic conditions. This reagent streamlines access to advanced intermediates in medicinal chemistry campaigns involving nitrogen heterocycles.

Application

tert-Butyl ((2-bromopyridin-4-yl)methyl)carbamate serves as a versatile building block for the synthesis of pyridyl-containing pharmaceutical intermediates. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the Boc-protected amine offers stability and ease of manipulation. This compound facilitates efficient access to functionalized heterocycles via standard deprotection and coupling protocols, making it well-suited for medicinal chemistry campaigns requiring late-stage diversification.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   51.22
  • LogP   2.8688
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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