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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511605Generated: October 25, 2026

N-(2-amino-4-chloro-5-(trifluoromethyl)phenyl)-3-(3-oxocyclobutyl)propanamide → HCID 178515984, compound

https://huagongshe.com/reaction/511605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-amino-4-chloro-5-(trifluoromethyl)phenyl)-3-(3-oxocyclobutyl)propanamideHCID 67773908—
SolventAcetic AcidHCID 176—
ProductHCID 178515984HCID 17851598466.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

N-(2-amino-4-chloro-5-(trifluoromethyl)phenyl)-3-(3-oxocyclobutyl)propanamide (72 mg, mmol) was taken up in acetic acid (3.2 mL) and the solution was heated at 65° C. for 26 h, upon which HPLC indicated the starting material was consumed and a new product had formed. The reaction mixture was cooled and the solvent was removed under high vac. The light brown residue was taken up in 20 mL ethyl acetate and the organic phase was washed with 10 mL portions of sat NaHCO3 and H2O. The organic phase was dried over Na2SO4, filtered and concentrated to yield a light brown glass. The crude material was purified by prep TLC (20 cm×20 cm×1.0 mm prep TLC plate, 3% MeOH/EA) to yield the title compound (45 mg, 66%) as a tan glass: MS (ESI+) for C14H12ClF3N2O m/z 317.2 (M+H)+; MS (ESI−) for C14H12ClF3N2O m/z 315.2 (M−H)−; HPLC purity 84.1% (ret. time, 2.98 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096634B2
Source datasetuspto-grants-2015_08
ORD IDord-ef64d264029148b2b8c93d8b2b8d5684
Source noteuspto-grants-2015_08