Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927631Generated: November 2, 2026

Hydrochloric Acid → HCID 58870822, compound

https://huagongshe.com/reaction/1927631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-chloro-N,N-diethyl-2-phenylacetamideHCID 4962500—
ReactantHCID 69304058HCID 69304058—
SolventMethanolHCID 887—
ProductHCID 58870822HCID 5887082221%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-[4-(2-ethyl-butyrylamino)-2-fluoro-phenyl]-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (96 mg, 0.25 mmol) in MeOH (5 mL) was added HCl (2 mL, 1 M in Et2O). After 16 h at 25° C., the mixture was concentrated and the residue re-dissolved in DMF (2 mL). The solution was treated with 2-chloro-N,N-diethyl-2-phenyl-acetamide (225 mg, 0.32 mmol) and K2CO3 (138 mg, 1.0 mmol), and was stirred at 25° C. for 16 h. The resulting mixture was purified by PTLC to provide the title compound (25 mg, 21%). MS: 480.4. 1H NMR (CDCl3): 7.57-7.45 (m, 3H), 7.40-7.27 (m, 4H), 7.20-7.06 (m, 2H), 5.90 (s, 1H), 4.43 (s, 1H), 3.55-3.15 (m, 6H), 2.92-2.83 (m, 1H), 2.74-2.64 (m, 1H), 2.53-2.44 (m, 2H), 2.07-1.98 (m, 1H), 1.76-1.47 (m, 4H), 1.17-0.90 (m, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183239B2
Source datasetuspto-grants-2012_05
ORD IDord-40231f8c57d94cc5a3925e3d5813df50
Source noteuspto-grants-2012_05