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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266302Generated: November 1, 2026

Trimethylsilyldiazomethane → Methyl 5-(boc-amino)-2-chloropyridine-4-carboxylate

https://huagongshe.com/reaction/1266302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant5-tert-Butoxycarbonylamino-2-chloroisonicotinic acidHCID 10564144—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductMethyl 5-(boc-amino)-2-chloropyridine-4-carboxylateHCID 53419715100%

Reaction Steps

To 5.4 g of 5-tert-butoxycarbonylamino-2-chloro-isonicotinic acid in 50 mL of methanol and 100 mL of chloroform was at 0° C. was added 15 mL of 2 M (trimethylsilyl)diazomethane in hexanes. After allowing the reaction to warm to ambient temperature and stirring for 2 hours, the solvents were removed and the crude product purified by passing through a plug of silica gel with chloroform. The product was then recrystallized from hexanes to give 5.8 g (100%) of 5-tert-butoxycarbonylamino-2-chloro-isonicotinic acid, methyl ester: mp=90-96° C. (decomposed); mass spectrum (m/e): M+H 287.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548496B2
Source datasetuspto-grants-2003_04
ORD IDord-2326e7f4a83246e998d118dccf026ef1
Source noteuspto-grants-2003_04