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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928427Generated: November 1, 2026

Toluene → Ethyl 1-((1-methyl-1,2,3,4-tetrahydroquinolin-7-yl)methyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/928427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl 1H-pyrazole-4-carboxylateHCID 142179—
ReactantSodium BicarbonateHCID 516892—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(1-Methyl-1,2,3,4-tetrahydroquinolin-7-yl)methanolHCID 58081183—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-((1-methyl-1,2,3,4-tetrahydroquinolin-7-yl)methyl)-1H-pyrazole-4-carboxylateHCID 58081247—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred, cooled (0° C.) solution of (1-methyl-1,2,3,4-tetrahydroquinolin-7-yl)methanol (200 mg, 0.733 mmol), ethyl 1H-pyrazole-4-carboxylate (103 mg, 0.733 mmol) and triphenylphosphine (289 mg, 1.100 mmol) in THF (10 ml) was added dropwise a 40% solution of DEAD in toluene (0.435 ml, 1.1 mmol). The reaction mixture was stirred for 2 h at 0° C., then over night at 20° C. Saturated aqueous NaHCO3 was added and the mixture was extracted with AcOEt. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound. The crude product was purified by preparative HPLC (Waters SunFire Prep C18 OBD 5 μm 30*100, Flow 40 mL/min, ACN: 2 min at 5%, then to 100% within 17.5 min, RT 10.00 min) to give the title compound. HPLC (Method H) Rt=2.919 min; MS (Method A) [M+H]+=300.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290485B2
Source datasetuspto-grants-2016_03
ORD IDord-a9f2698a60b649c69f57f9337a2affd9
Source noteuspto-grants-2016_03