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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171231Generated: November 2, 2026

tert-Butanol → Tert-butyl (5-fluoro-6-methoxypyridin-3-yl)carbamate

https://huagongshe.com/reaction/2171231

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-Fluoro-6-methoxynicotinic acidHCID 55265267—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductTert-butyl (5-fluoro-6-methoxypyridin-3-yl)carbamateHCID 89546885—

Reaction Steps

Triethylamine (267 μl), tert-butanol (230 μl), and DPPA (413 μl) were added to a toluene (5 ml) solution containing 5-fluoro-6-methoxynicotinic acid (275 mg), followed by reflux for 3 hours. The reaction solution was adjusted to room temperature and water was added, followed by extraction with ethyl acetate. Next, the organic layers were washed with saturated saline and dried over anhydrous sodium sulfate and the solvent was distilled away under reduced pressure. Then, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=10:1 to 3:1). Colorless oily matter of tert-butyl (5-fluoro-6-methoxypyridin-3-yl)carbamate (279 mg) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051310B2
Source datasetuspto-grants-2015_06
ORD IDord-e9a87702383740e3b3aa45a141bf50f8
Source noteuspto-grants-2015_06