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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846650Generated: November 2, 2026

Triethylamine → HCID 67322638, compound

https://huagongshe.com/reaction/1846650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-MethylhomopiperazineHCID 228349—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 68304426HCID 68304426—
SolventDimethylformamideHCID 6228—
ProductHCID 67322638HCID 6732263875.1%

Reaction Steps

A mixture of 0.035 g (0.078 mmol) of [3′-(3-chloro-benzoylamino)-5′-phenyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl]-acetic acid, 0.044 g (0.39 mmol) of 1-methyl homopiperazine, 0.032 g (0.10 mmol) of O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate, and 0.032 mL (0.23 mmol) of triethylamine in N,N-dimethylformamide (2 mL) are stirred overnight at room temperature. The mixture is concentrated under reduced pressure and the residue is diluted with water which causes a solid to precipitate from solution. The colorless solid is collected by filtration, washed with water and dried to provide 0.032 g (75%) of 3-chloro-N-(2-{4-[2-(4-methyl-1,4-diazepan-1-yl)-2-oxoethyl]piperidin-1-yl}-5-phenylpyridin-3-yl)benzamide (124) as a colorless solid. [M+H]+=546.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952004B2
Source datasetuspto-grants-2015_02
ORD IDord-e0b8a9d42c37473fa25b665d7c78d290
Source noteuspto-grants-2015_02