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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750460Generated: October 25, 2026

Hydrochloric Acid → HCID 118308256, compound

https://huagongshe.com/reaction/1750460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
Reactant(1S,2S)-trans-N-Boc-1,2-cyclopentanediamineHCID 17040218—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
ProductHCID 118308256HCID 118308256—

Reaction Conditions

Temperature140 °C

Reaction Steps

A microwave vial was charged with tert-butyl N-[(1S,2S)-2-aminocyclopentyl]carbamate (CAS number 586961-34-4; 1.0 g, 4.99 mmol), 2-chloro-5-(trifluoromethyl)pyridine (CAS number 52334-81-3; 0.997 g, 5.49 mmol), DIPEA (2.62 ml, 14.98 mmol) and DMSO (16.6 ml). The reaction was heated with microwave irradiation at 140° C. for 2 hours and then partitioned between ethyl acetate and water. The organics were washed with water and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. This was then purified by column chromatography (silica, 0-50% ethyl acetate/petrol) to afford a cream solid to which was then added methanol (10 ml) and HCl in 1,4-dioxane (4M, 6.24 ml, 24.97 mmol) and the reaction was stirred at room temperature for 17 hours. The reaction mixture was concentrated in vacuo and azeotropically distilled with toluene to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156829B2
Source datasetuspto-grants-2015_10
ORD IDord-adfe6d8e595d40458419aeedf13db212
Source noteuspto-grants-2015_10