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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77102Generated: October 26, 2026

N,1-dimethylpyrrolidin-3-amine → HCID 178480456, compound

https://huagongshe.com/reaction/77102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,1-dimethylpyrrolidin-3-amineHCID 2758520—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 178479749HCID 178479749—
ProductHCID 178480456HCID 17848045630%

Reaction Conditions

Temperature35 °C

Reaction Steps

Method J—Step a To a mixture of 1-[3-(5-Chloro-1H-benzoimidazol-2-yl)-4-fluoro-phenyl]-piperidine-4-carboxylic acid hydrochloride (obtained as described in general method 10, step b) (0.01 g, 0.25 mmol) in dcm (2 mL), HATU (0.10 g, 0.26 mmol), TEA (0.07 mL, 0.55 mmol) and N,N′-dimethyl-3-aminopyrrolidine (0.04 g, 0.31 mmol) were added. The reaction mixture was heated at 35° C. overnight, cooled to room temperature and washed with ammonium chloride solution (2 mL), saturated Na2CO3 solution (2 mL) and water (2 mL). The organic layer was then filtrated on an NH2 cartridge and further purified by flash chromatography (eluent: EtOAc:NH3 2N in MeOH/9:1) to obtain 0.03 g of the title compound (30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835648B2
Source datasetuspto-grants-2014_09
ORD IDord-5a847595c8984844a698703d86c9781a
Source noteuspto-grants-2014_09