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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747245Generated: November 3, 2026

Sodium Bicarbonate → Tert-butyl 4-(3-(3-(6-methylpyridin-3-yl)ureido)phenethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1747245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-Isocyanato-2-methylpyridineHCID 7330505—
ReactantTert-butyl 4-(3-aminophenethyl)piperazine-1-carboxylateHCID 57597088—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(3-(3-(6-methylpyridin-3-yl)ureido)phenethyl)piperazine-1-carboxylateHCID 5759710563%

Reaction Steps

To a solution of tert-butyl 4-(3-aminophenethyl)piperazine-1-carboxylate (7D, 1.0 eq) in THF (about 0.3 M 7D in THF) was added 5-isocyanato-2-methylpyridine (1.0 eq) dropwise. The resulting reaction mixture was stirred for 2 h. To the reaction mixture was added saturated aq. NaHCO3. The mixture was diluted with EtOAc, and the layers were separated. The organic layer was washed twice with saturated aq. NaHCO3 and once with brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. Purification over silica gel using 5-12% MeOH/CH2Cl2 as the gradient eluant provided tert-butyl 4-(3-(3-(6-methylpyridin-3-yl)ureido)phenethyl)piperazine-1-carboxylate (7E, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150564B2
Source datasetuspto-grants-2015_10
ORD IDord-115586c30ef6421780d9d0836206f736
Source noteuspto-grants-2015_10