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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174373Generated: October 31, 2026

Hydrochloric Acid → HCID 66549041, compound

https://huagongshe.com/reaction/2174373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2,2-Trifluoroethylamine hydrochlorideHCID 9772—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 86707793HCID 86707793—
SolventDimethylformamideHCID 6228—
ProductHCID 66549041HCID 6654904152%

Reaction Steps

To a stirred solution of 3-Fluoro-3-{4-[5-(3,4,5-trichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-phenyl}-cyclobutanecarboxylic acid (Preparation 6, 0.1 g, 0.195 mmol) in DMF (3 mL) was added HOBt (0.027 g, 0.195 mmol) and DIPEA (0.050 g, 0.391 mmol) followed by addition of EDCl.HCl (0.056 g, 0.292 mmol) and 2,2,2-trifluoro-ethylamine hydrochloride (0.026 g, 0.195 mmol) at 0° C. Resulting reaction mixture was stirred at room temperature for 16 hours under nitrogen atmosphere. After complete consumption of starting material, reaction mixture was quenched with water (50 mL) and extracted with EtOAc (3×20 mL). Combined organic layer was washed with saturated NaHCO3 (2×50 mL), dried over sodium sulphate and evaporated in vacuo to get 0.150 g crude. Crude was purified by column chromatography on silica gel (100-200 mesh size). Compound was eluted using 0.8% methanol in DCM to afford white solid (0.060 g, 52%). 1H-NMR (400 MHz, CDCl3) δ: 2.80-2.90 (m, 3H), 2.91-2.98 (m, 1H), 3.30-3.39 (m, 1H), 3.67 (d, 1H, J=17.16 Hz), 3.90-3.99 (m, 2H), 4.07 (d, 1H, J=17.16 Hz), 5.71 (bs, 1H), 7.53 (d, 2H, J=8.32 Hz), 7.64-7.67 (m, 4H); LC-MS (m/z): [M−H] 588.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061013B2
Source datasetuspto-grants-2015_06
ORD IDord-47ec2ef5c3d7442995c2e541f7bb9820
Source noteuspto-grants-2015_06