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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108078Generated: October 31, 2026

Ammonium Bicarbonate → HCID 18786356, compound

https://huagongshe.com/reaction/1108078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium BicarbonateHCID 14013—
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
ReactantHCID 18786346HCID 18786346—
SolventDichloromethaneHCID 6344—
ProductHCID 18786356HCID 1878635654.2%

Reaction Steps

A suspension of 4-[3-[4-(pyrrol-1-ylmethyl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylic acid (0.36 g, 0.93 mmol), ammonium bicarbonate (0.44 g, 5.58 mmol) and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (0.28 g, 1.12 mmol) in dichloromethane (20 ml) were stirred at room temperature overnight. Ammonium bicarbonate and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline were added until the acid was consumed. The reaction mixture was diluted with dichloromethane (50 ml) and washed with water (50 ml). The organic extract was washed with cold 1N hydrochloric acid (50 ml), water (50 ml) and saturated aqueous sodium bicarbonate (5 ml), water (50 ml) and brine (50 ml), dried (magnesium sulfate) and concentrated to dryness. Recrystallization of the residue from ethyl acetate afforded the titled compound (198 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063928
Source datasetuspto-grants-2000_05
ORD IDord-790f758284e04288adb9fa29e489ff43
Source noteuspto-grants-2000_05