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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958092Generated: November 2, 2026

Triethylamine → Methyl 4-(4-(3-(6-methylpyridin-3-yl)ureido)-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1958092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Isocyanato-2-methylpyridineHCID 7330505—
Reactantmethyl 4-(4-amino-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylateHCID 59302728—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-(4-(3-(6-methylpyridin-3-yl)ureido)-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylateHCID 1156057651.1%

Reaction Steps

To a room temperature solution of Methyl 4-(4-amino-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylate (175 mg, 0.635 mmol, 1.0 equiv) and triethylamine (90 μL, 0.635 mmol, 1.0 equiv) in dry DCM (1.7 mL) was added freshly filtered 2-methyl-5-isocyanatopyridine (94 mg, 0.699 mmol, 1.1 equiv) in dry DCM (1.7 mL) dropwise via cannula. After 1 h, the reaction was diluted with DCM and washed with water and with brine. The resulting solution was dried over sodium sulfate, filtered, and concentrated in vacuo. The solid was dissolved in a minimal volume of DMF and water was added to precipitate the product. The resulting solid was filtered, washed three times with water and twice with hexane to provide the title compound as a light brown solid (133 mg, 51%). LCMS [M+H]+=410.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410108B2
Source datasetuspto-grants-2013_04
ORD IDord-f91a5ab6c447493f9a76cb25185218e9
Source noteuspto-grants-2013_04