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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929298Generated: November 1, 2026

Lithium Hexamethyldisilazide → HCID 86700608, compound

https://huagongshe.com/reaction/929298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(1R,4S)-tert-Butyl 3-oxo-2-azabicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 11830665—
ReactantHCID 67499849HCID 67499849—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86700608HCID 86700608—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3-chloro-N-methyl-1-(pyridin-3-yl)-1H-pyrazol-4-amine (0.20 g, 0.96 mmol) in THF (10 mL) was cooled to a temperature of about −78° C. LHMDS (1 M solution in hexanes, 1.0 mL, 1.00 mmol) was added, and the solution was stirred at a temperature of about −78° C. for 15 minutes. A solution of (1R,4S)-tert-butyl 3-oxo-2-azabicyclo[2.2.1]hept-5-ene-2- carboxylate (0.20 g, 0.96 mmol) dissolved in THF (3 mL) was added to the solution at a temperature of about −78° C. in one portion. After stirring for one hour at a temperature of about −78° C., the cooling bath was removed and the reaction warmed to a temperature of about 20° C. After stirring for an additional five minutes, acetic acid (AcOH, 0.1 mL) was added to the solution. The reaction mixture was concentrated and purified via silica gel chromatography eluting with EtOAc/hexanes to give the title compound F109 as a white solid (0.25 g, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09295260B2
Source datasetuspto-grants-2016_03
ORD IDord-e9915baf093042bbbdd65d79489367cd
Source noteuspto-grants-2016_03