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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181549Generated: October 31, 2026

2-Amino-5-bromopyridine → HCID 178426926, compound

https://huagongshe.com/reaction/1181549

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 178469061HCID 178469061—
SolventDichloromethaneHCID 6344—
ProductHCID 178426926HCID 17842692649.1%

Reaction Steps

A solution of 2-amino-5-bromopyridine (0.200 g, 1.16 mmol 1.0 equiv), in 5 mls of methylene chloride, under argon, was treated with trimethylaluminum (0.312 mL, 2.0N in hexanes, 4.0 equiv) at room temperature for 30 min. To the solution was added ethyl-3-methylpyrazole-5-carboxylate (0.356 g, 2.0 equiv). After 4 hrs, the volatile was evaporated, and the residue was redissolved into EtOAc, washed with 0.5N HCl, 0.2 N K2CO3, and saturated aqueous NaCl. The organic layer was dried over Na2SO4, filtered, evaporated and purified via flash chromatography on silica gel to give N-(5-bromo-2-pyridinyl)-(3-methyl)-5-pyrazolecarboxamide (0.160 g, 49%). MS found for C10H9BrN4O (M+H)+: 281, 283.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285565B2
Source datasetuspto-grants-2007_10
ORD IDord-3583181ee6084b4da2519154f7028b81
Source noteuspto-grants-2007_10