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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425754Generated: October 27, 2026

Triethylamine → HCID 67246672, compound

https://huagongshe.com/reaction/2425754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 2-bromopropanoateHCID 545327—
ReactantHCID 67245033HCID 67245033—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67246672HCID 6724667265%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-isopropyl-5-methyl-2-oxo-N-(piperidin-4-ylmethyl)-1,2-dihydroquinoline-3-carboxamide hydrochloride (467 mg, 0.98 mmol, step 4 in preparation 3), tert-butyl 2-bromopropanoate (0.24 mL, 1.47 mmol), and triethylamine (0.41 mL, 2.93 mmol) in tetrahydrofuran (30 mL) was stirred at 70° C. for 23 h. After cooling to room temperature, the mixture was poured onto saturated aqueous sodium hydrogen carbonate (100 mL), and the aqueous layer was extracted with dichloromethane (100 mL×2). The combined organic layer was dried over magnesium sulfate, and concentrated in vacuo. The residue was chromatographed on a column of silica gel eluting with ammonia/methanol/dichloromethane (0.1:1:30) to give 299 mg (65%) of the title compound as a yellow amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964727B2
Source datasetuspto-grants-2011_06
ORD IDord-1a376291ffd84bd0a2b74d0c6dc488c9
Source noteuspto-grants-2011_06