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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441840Generated: October 27, 2026

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

https://huagongshe.com/reaction/1441840

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 numberUS07655689B2
Source datasetuspto-grants-2010_02
ORD IDord-23817901c61c42f2a446cf2b028513fc
Source noteuspto-grants-2010_02