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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666334Generated: October 26, 2026

Pyridine → Phenyl 6-methoxypyridin-3-ylcarbamate

https://huagongshe.com/reaction/1666334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTetrahydrofuranHCID 8028—
ReactantPhenyl chloroformateHCID 15891—
Reactant5-Methoxypyridin-3-ylamineHCID 12703595—
ProductPhenyl 6-methoxypyridin-3-ylcarbamateHCID 2018596296%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Amino-5-methoxy-pyridine (5.00 g, 40.3 mmol) was dissolved in THF (80 mL), cooled to 0° C., treated with pyridine (4.07 mL, 50.4 mmol) followed by phenylchloroformate (5.32 mL, 42.3 mmol). The reaction mixture was slowly warmed to RT over several hours and stirred an additional 12 h. The mixture was partitioned between water and EtOAc. The organic layer was separated and the aqueous layer was extracted again. The combined organic extracts were dried over sodium sulfate, filtered and concentrated to give the product as a reddish solid (9.45 g, 96%), which was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-bf15aa18ac8640bd9f5cd0e1d19e0ffa
Source noteuspto-grants-2011_10