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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551805Generated: October 31, 2026

Diisopropylethylamine → HCID 67187228, compound

https://huagongshe.com/reaction/551805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67188496HCID 67188496—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 67187228HCID 6718722875.6%

Reaction Steps

0.25 g of 1-[(3-(pyridin-3-yl)pyrrolidin-1-yl)carbonyl]-1,2,3,4-tetrahydroquinoxaline, 8.1 ml of dichloromethane and 0.3 ml of diisopropylethylamine are placed in a 50 ml round-bottomed flask under a nitrogen atmosphere. 0.12 g of triphosgene is added at 0° C. and then the reaction mixture is left stirring at ambient temperature for three hours. 0.5 ml of diisopropylethylamine and 0.33 ml of methanol are subsequently added and the reaction mixture is stirred for twenty-four hours. A saturated aqueous sodium hydrogencarbonate solution and dichloromethane are added. The aqueous phase is extracted three times with dichloromethane. The organic phases are combined, washed with water and with a saturated aqueous sodium chloride solution and dried over sodium sulfate and then the solvent is evaporated under reduced pressure. The residue is chromatographed on silica gel with a dichloromethane/methanol 95/5 mixture. 0.112 g of methyl 4-[(3-(pyridin-3-yl)pyrrolidin-1-yl)carbonyl]-3,4-dihydroquinoxaline-1(2H)-carboxylate is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947834B2
Source datasetuspto-grants-2011_05
ORD IDord-bb200ce2fc1344cf9b19470e82388d9c
Source noteuspto-grants-2011_05