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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241805Generated: November 1, 2026

Triethylamine → tert-Butyl 4-((4-(3-(6-methylpyridin-3-yl)ureido)benzo[d]oxazol-2-yl)methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/241805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Isocyanato-2-methylpyridineHCID 7330505—
Reactanttert-Butyl 4-((4-aminobenzo[d]oxazol-2-yl)methyl)piperazine-1-carboxylateHCID 59302726—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-((4-(3-(6-methylpyridin-3-yl)ureido)benzo[d]oxazol-2-yl)methyl)piperazine-1-carboxylateHCID 23654605100%

Reaction Steps

To a room temperature solution of tert-butyl 4-((4-aminobenzo[d]oxazol-2-yl)methyl)piperazine-1-carboxylate (5.0 g, 15.1 mmol, 1.0 equiv) and triethylamine (2.1 g, 15.1 mmol, 1.0 equiv) in dry DCM (37 mL) was added 2-methyl-5-isocyanatopyridine (2.22 g, 16.6 mmol, 1.1 equiv) in dry DCM (37 mL) via cannula. After 1 h, the reaction mixture was filtered and washed with water (25 mL) and brine (25 mL). The solution was dried over sodium sulfate, filtered and concentrated in vacuo. Silica gel purification (5% MeOH/95% EtOAc—15% MeOH/85% EtOAc) provided the title compound as a white foam (7.03 g, 100%). LCMS [M+H]+=467.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653081B2
Source datasetuspto-grants-2014_02
ORD IDord-2bc9b1d91be945c48bdeeb0cc42ebf8d
Source noteuspto-grants-2014_02