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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675751Generated: October 29, 2026

Triethylamine → tert-Butyl (2-oxo-3-pyrimidin-4-yl-2,3-dihydro-1H-benzimidazol-1-yl)acetate

https://huagongshe.com/reaction/1675751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl [3-(6-chloropyrimidin-4-yl)-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl]acetateHCID 86607781—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl (2-oxo-3-pyrimidin-4-yl-2,3-dihydro-1H-benzimidazol-1-yl)acetateHCID 86607782—

Reaction Steps

A mixture of tert-butyl[3-(6-chloropyrimidin-4-yl)-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl]acetate from Step A (260 mg, 0.720 mmol), 10% Pd/C (23 mg) and triethylamine (0.150 mL, 1.08 mmol) in EtOH (5 mL) was stirred under an atmosphere of hydrogen (ca. 1 atm) for 2 h. The mixture was filtered through a pad of Celite, washing with EtOH, and the filtrate was concentrated to give the title compound. MS: m/z=327 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003792B2
Source datasetuspto-grants-2011_08
ORD IDord-a6754c131c6f409bb7b991b59fcd3016
Source noteuspto-grants-2011_08