Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770823Generated: November 1, 2026

Pyridine → 6-Bromo-2-(tert-butylcarbonyl)amino-3-methoxypyridine

https://huagongshe.com/reaction/1770823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPivaloyl chlorideHCID 62493—
Reactant2-Amino-6-bromo-3-methoxypyridineHCID 57562906—
SolventDichloromethaneHCID 6344—
Product6-Bromo-2-(tert-butylcarbonyl)amino-3-methoxypyridineHCID 57562884—

Reaction Steps

A dry reaction flask equipped with a nitrogen inlet and magnetic stirring bar was charged with 2-amino-6-bromo-3-methoxypyridine (33) (0.170 g, 0.84 mmol), pyridine (0.126 mL, 1.26 mmol) and CH2Cl2 (5 mL). To this at 0° C. was added pivaloyl chloride (0.113 mL, 0.92 mmol) and then the reaction mixture was stirred at room temperature overnight. The reaction was then quenched with water (25 mL), extracted with CH2Cl2 (2×25 mL), dried over anhydrous sodium sulfate and solvent was removed under reduced pressure to afford 6-bromo-2-(tert-butylcarbonyl)amino-3-methoxypyridine (34). LCMS: purity: 80%; MS (m/z): 287 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248190B2
Source datasetuspto-grants-2016_02
ORD IDord-c65cf7d72d55458581cfa4b08903f27a
Source noteuspto-grants-2016_02