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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966935Generated: October 26, 2026

Potassium Carbonate → (4-Oxazol-5-yl-naphthalen-1-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/966935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantToluene-sulfonylisocyanideHCID 21875242—
Reactant(4-Cyano-naphthalen-1-yl)-carbamic acid tert-butyl esterHCID 58745930—
Reactanttert-Butyl 4-formylnaphthalen-1-ylcarbamateHCID 58745967—
SolventMethanolHCID 887—
Product(4-Oxazol-5-yl-naphthalen-1-yl)-carbamic acid tert-butyl esterHCID 5874584844%

Reaction Steps

The above mixture of compounds 503A & 503B (3.37 g, 10.0 mmol; corrected for presence of compound 503A), toluene-sulfonylisocyanide (2.15 g, 11.0 mmol) and potassium carbonate (1.66 g, 12.0 mmol) in 50 mL of methanol was refluxed for 4 h. The reaction mixture was partitioned between water (200 mL) and chloroform (200 mL). After extracting the aqueous layer with chloroform (100 mL), the combined organic layers were dried over magnesium sulfate and concentrated in vacuo. The crude residue was purified by flash chromatography on silica gel eluting with a gradient of 10-40% ethyl acetate in hexane to give 1.35 g (44%) of compound 503C as a white solid. 1HNMR (400 MHz, DMSO-d6): δ 9.45 (s, 1H), 8.57 (s, 1H), 8.20 (m, 2H), 7.76 (m, 2H), 7.64 (s, 1H), 7.62 (m, 2H), 1.51 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953679B2
Source datasetuspto-grants-2005_10
ORD IDord-a3244177f8ab4cb782c0ec0c8935a529
Source noteuspto-grants-2005_10