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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396403Generated: October 29, 2026

HCID 9944444, compound → HCID 10272449, compound

https://huagongshe.com/reaction/396403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 9944444HCID 9944444—
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10272449HCID 10272449—

Reaction Conditions

Temperature-15 °C

Reaction Steps

A −15° C. solution of N-BOC propargyl amine (641 mg, 4.13 mmole, 3.5 eq) in dry THF (12 ml) was treated dropwise with a 1.6M n-BuLi in hexanes solution (5.16 ml, 8.3 mmole, 7.0 eq) and the resulting pale yellow dianion solution stirred at −15° C. for 30 minutes under nitrogen. A dry THF solution (3 ml) of the above-prepared 2,4-Diphenyl-oxazole-5-carboxylic acid methoxy-methyl-amide (365 mg, 1.18 mmole, 1.0 eq) was added dropwise to the dianion solution at −15° C. and the mixture stirred at 0° C. for 2 hours under nitrogen. The mixture was quenched by adding a solution of 2M NaH2PO4 (5 ml), then warmed to room temperature and extracted with ethyl acetate. The organic phase was washed with water and brine then dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound as a crude brown oil. The crude oil without purification was used immediately in next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608087B1
Source datasetuspto-grants-2003_08
ORD IDord-d28d5f93e57946f483768dd27e39f48f
Source noteuspto-grants-2003_08