tert-Butyl 4-(6-bromo-[1, 2, 4]triazolo[1, 5-a]pyridin-2-yl)piperidine-1-carboxylate
97%
- Product Code: 152058
CAS:
1422344-42-0
| Molecular Weight: | 381.27 g./mol | Molecular Formula: | C₁₆H₂₁BrN₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23378329 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of complex heterocyclic systems found in drug candidates targeting inflammation, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides protection for the piperidine nitrogen during multi-step syntheses, allowing selective reactions at other sites. The bromo-triazolopyridine moiety serves as a handle for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations, enabling rapid diversification in medicinal chemistry campaigns.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | Ft84,906.83 |
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tert-Butyl 4-(6-bromo-[1, 2, 4]triazolo[1, 5-a]pyridin-2-yl)piperidine-1-carboxylate
Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of complex heterocyclic systems found in drug candidates targeting inflammation, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides protection for the piperidine nitrogen during multi-step syntheses, allowing selective reactions at other sites. The bromo-triazolopyridine moiety serves as a handle for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations, enabling rapid diversification in medicinal chemistry campaigns.
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