Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735803Generated: October 30, 2026

Diisopropylethylamine → HCID 58980644, compound

https://huagongshe.com/reaction/735803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantEthyl 2-bromo-6-(1,1-dimethylethyl)-3-hydroxy-4-pyridinecarboxylateHCID 58980648—
SolventAcetonitrile methanolHCID 21959252—
ProductHCID 58980644HCID 5898064493%

Reaction Steps

To a solution of the above bromopyridine (2.74 g, 9.07 mmol) in acetonitrile/methanol (9:1, 33 mL) was added N,N-diisopropylethylamine (2.50 mL, 14.2 mmol) followed by (trimethylsilyl)diazomethane (2.0M in hexane, 7.0 mL, 14.2 mmol). The red solution was stirred 0.5 h at room temperature then concentrated in vacuo. The residue was dissolved in methylene chloride, washed with saturated aqueous NaHCO3, dried over sodium sulfate, filtered, and concentrated in vacuo to provide 2-bromo-6-tert-butyl-3-methoxy-isonicotinic acid ethyl ester (2.65 g, 93%) as a red oil which was utilized without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592332B2
Source datasetuspto-grants-2009_09
ORD IDord-d3959b4ecab84203864e32467d187703
Source noteuspto-grants-2009_09