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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403274Generated: October 31, 2026

Hydrochloric Acid → HCID 68325405, compound

https://huagongshe.com/reaction/2403274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 68325504HCID 68325504—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
SolventTetrahydrofuran ethyl acetateHCID 21939870—
ProductHCID 68325405HCID 6832540556%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of (RS)-3-{4-[(RS)-1-(5-bromo-pyridin-2-yl)-2,2,2-trifluoro-ethylamino]-phenyl}-pyrrolidine-1-carboxylic acid tert-butyl ester (27 mg) in THF (1 ml) was added dropwise a solution of hydrogen chloride in dioxane (0.20 ml, 4 M solution) and the mixture was heated at 60° C. for 4 hours. The mixture was then cooled to room temperature, diluted with ethyl acetate/THF (1:1), and washed sequentially with 2 N aq. sodium hydroxide solution and with saturated brine. The organic phase was separated, dried over sodium sulphate, and concentrated in vacuo. The reside was purified by flash column chromatography (silical gel; gradient: heptane/dichloromethane/methanol) to give [(RS)-1-(5-bromo-pyridin-2-yl)-2,2,2-trifluoro-ethyl]-((RS)-4-pyrrolidin-3-yl-phenyl)-amine (12 mg, 56%) as a yellow amorphous solid. MS (ISP): 402.1 ([{81Br}M+H]+), 400.1 ([{79Br}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802673B2
Source datasetuspto-grants-2014_08
ORD IDord-190b30c02a0040959a48acf4c7518b84
Source noteuspto-grants-2014_08