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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 511605생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/511605

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참여 물질

역할이름HCID투입량
반응물N-(2-amino-4-chloro-5-(trifluoromethyl)phenyl)-3-(3-oxocyclobutyl)propanamideHCID 67773908—
용매Acetic AcidHCID 176—
생성물HCID 178515984HCID 17851598466.1%

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온도65 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096634B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-ef64d264029148b2b8c93d8b2b8d5684
출처 메모uspto-grants-2015_08