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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408487Generated: October 30, 2026

Ethyl Acetate → HCID 67053852, compound

https://huagongshe.com/reaction/2408487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant1-Boc-3-hydroxypiperidineHCID 545699—
ReactantHCID 86670628HCID 86670628—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67053852HCID 6705385260.2%

Reaction Steps

tert-Butyl 3-hydroxypiperidine-1-carboxylate (100 mg, 0.5 mmol) was dissolved in dry NMP (5 mL) and NaH (20 mg, 60% in oil, 0.5 mmol) was added carefully. The mixture was stirred at room temperature for 10 min. Then, ethyl 4-chloro-2-(3-fluorophenyl)thieno[2,3-d]pyridazine-7-carboxylate (130 mg, 0.5 mmol) was added. The mixture was heated up to 80° C. and stirred for 30 min. After cooling to room temperature, EtOAc was added to dilute the reaction and washed with water and brine. The organics was dried over Na2SO4 and filtered, concentrated. The crude product was purified with column (silica gel) to give the product ethyl 4-(1-(tert-butoxycarbonyl)piperidin-3-yloxy)-2-(3-fluorophenyl)thieno[2,3-d]pyridazine-7-carboxylate (151 mg). HPLC-MS tR=2.17 min (UV254 nm); mass calculated for formula C25H28FN3O5S 501.2, observed LCMS m/z 502.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815863B2
Source datasetuspto-grants-2014_08
ORD IDord-1282a46b5a964bf58b2bdb017c92a650
Source noteuspto-grants-2014_08