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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551814Generated: October 27, 2026

Diisopropylethylamine → HCID 67188217, compound

https://huagongshe.com/reaction/551814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
Reactant3-(Pyrrolidin-3-yl)pyridineHCID 3613651—
ReactantMethyl 1,2,3,4-tetrahydroquinoline-6-carboxylate hydrochlorideHCID 67188214—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 67188217HCID 67188217176.8%

Reaction Steps

0.6 g of methyl 1,2,3,4-tetrahydroquinoline-6-carboxylate hydrochloride, 13.2 ml of dichloromethane and 2.54 ml of diisopropylethylamine are placed in a 100 ml round-bottomed flask under a nitrogen atmosphere. 0.31 g of triphosgene is added at 0° C. and then the reaction mixture is left stirring at ambient temperature for three hours. 0.39 g of 3-(pyrrolidin-3-yl)pyridine is subsequently added and the reaction mixture is stirred for eighteen hours. Water 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. 0.675 g of methyl 1-[(3-(pyridin-3-yl)pyrrolidin-1-yl)carbonyl]-1,2,3,4-tetrahydroquinoline-6-carboxylate is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947834B2
Source datasetuspto-grants-2011_05
ORD IDord-68a4bc36a97b4427b425601bea628e16
Source noteuspto-grants-2011_05