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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827547Generated: October 26, 2026

Triethylamine → HCID 22137343, compound

https://huagongshe.com/reaction/1827547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4,6-Trichlorobenzoyl chlorideHCID 2733703—
Reactant[4-(2-Pyrrolidin-1-yl-ethoxy)-phenyl]-[3-(tetrahydro-pyran-2-yloxy)-benzyl]-amineHCID 22137433—
SolventDichloromethaneHCID 6344—
ProductHCID 22137343HCID 22137343—

Reaction Steps

To a solution of [4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-[3-(tetrahydro-pyran-2-yloxy)-benzyl]-amine (0.050 g, 0.13 mmol) in 0.5 mL methylene chloride was added triethylamine (0.035 mL, 0.25 mmol), 2,4,6-trichlorobenzoyl chloride (0.061 g, 0.25 mmol), and catalytic N,N-dimethylaminopyridine (DMAP). The reaction mixture was stirred overnight at room temperature. The reaction was concentrated to give the title compound of Step A which was used in Step B without further purification. MS 605.4 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053212B2
Source datasetuspto-grants-2006_05
ORD IDord-4aece03e0bae4bb3847e2d9646f2a078
Source noteuspto-grants-2006_05