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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354079Generated: October 30, 2026

1,2-Dichloroethane → HCID 68690135, compound

https://huagongshe.com/reaction/2354079

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-BenzylpiperidineHCID 31738—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 58816583HCID 58816583—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 68690135HCID 68690135—

Reaction Steps

To a cooled (0° C.) mixture of [3-(2-methyl-pyridin-4-yl)-ureido]-acetic acid (Example D3., 105 mg, 0.5 mmol), 4-benzylpiperidine (Example A1., 105 mg, 0.6 mmol), HOBt (81 mg, 0.6 mmol), TEA (0.14 mL, 1 mmol) and a cat. amount of DMAP in CH2Cl2 (20 mL) are added, followed by EDC (115 mg, 0.6 mmol). The mixture is stirred at r.t. for 15 h. The mixture is quenched with sat. aq. Na2CO3 (25 mL), the phases are separated, and the aq. phase is extracted with CH2Cl2 (3×30 mL). The combined organic extracts are dried (Na2SO4), filtered and evaporated to provide the crude title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750161B2
Source datasetuspto-grants-2010_07
ORD IDord-cf322c6b041e4558adf711d9f51f1a9e
Source noteuspto-grants-2010_07