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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281250Generated: November 1, 2026

Triethylamine → N-(2-(4-bromophenyl)propan-2-yl)-2-(quinuclidin-3-yl)acetamide

https://huagongshe.com/reaction/2281250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-(4-Bromophenyl)propan-2-amineHCID 23009116—
Reactant2-(Quinuclidin-3-yl)acetic acid hydrochlorideHCID 23024147—
SolventDimethylformamideHCID 6228—
ProductN-(2-(4-bromophenyl)propan-2-yl)-2-(quinuclidin-3-yl)acetamideHCID 6832794976%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2-(quinuclidin-3-yl)acetic acid hydrochloride (0.97 g, 4.7 mmol) in DMF (30 mL) was added HATU (1.79 g, 4.72 mmol), 2-(4-bromophenyl)propan-2-amine (1.0 g, 4.7 mmol), and triethylamine (3.9 mL, 28 mmol). The resulting mixture was stirred at 60° C. for 16 h. The mixture was concentrated in vacuo, diluted with EtOAc and washed with brine. The organic layer was dried over Na2SO4 and evaporated to afford crude product, which was purified by silica gel column chromatography (EtOAc/methanol 50/1 to 3/1) to obtain N-(2-(4-bromophenyl)propan-2-yl)-2-(quinuclidin-3-yl)acetamide as a yellow solid (1.3 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139580B2
Source datasetuspto-grants-2015_09
ORD IDord-15844f54be8346cc81bc8d0aaeb2204f
Source noteuspto-grants-2015_09