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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 557802생성일: 2026년 10월 24일

Triethylamine → 3,3-Dimethyl-5-oxo-5-(3-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenoxy}-piperidin-1-yl)-pentanoic acid

https://huagongshe.com/ko/reaction/557802

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,3-Dimethylglutaric anhydrideHCID 77813—
반응물2-Phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid [4-(piperidin-3-yloxy)-phenyl]-amideHCID 57651879—
용매Dimethyl SulfoxideHCID 679—
생성물3,3-Dimethyl-5-oxo-5-(3-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenoxy}-piperidin-1-yl)-pentanoic acidHCID 2511794855.4%

반응 단계

2-Phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid [4-(piperidin-3-yloxy)-phenyl]-amide (46.2 mg, 0.107 mmol), 4,4-dimethyl-dihydro-pyran-2,6-dione (18.3 mg, 0.128 mmol) and triethylamine (30 uL, 0.214 mmol) in 1 mL DMSO were treated as above. The crude product was purified by flash chromatography to yield 3,3-dimethyl-5-oxo-5-(3-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenoxy}-piperidin-1-yl)-pentanoic acid as a white solid (34 mg, 55%). ES-MS calcd for C29H30F3N3O6 (m/e) 573.57, obsd 574 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08058299B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-c95ff24f8a524844ac53ea83ced212e9
출처 메모uspto-grants-2011_11