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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 557801생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/557801

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Dihydro-3,3-dimethyl-2H-pyran-2,6(3H)-dioneHCID 76247—
반응물2-Phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid [4-(piperidin-3-yloxy)-phenyl]-amideHCID 57651879—
용매Dimethyl SulfoxideHCID 679—
생성물2,2-Dimethyl-5-oxo-5-(3-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenoxy}-piperidin-1-yl)-pentanoic acidHCID 2512292856.4%

반응 단계

2-Phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid [4-(piperidin-3-yloxy)-phenyl]-amide (44.1 mg, 0.102 mmol), 3,3-dimethyl-dihydro-pyran-2,6-dione (17.5 mg, 0.122 mmol) and triethylamine (28.5 uL, 0.204 mmol) in 1 mL DMSO were treated as above. The crude product was purified by flash chromatography to yield 2,2-dimethyl-5-oxo-5-(3-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenoxy}-piperidin-1-yl)-pentanoic acid as a white solid (33 mg, 56%). 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-2f4de240e87f4a8daff98fb99f1eaa5b
출처 메모uspto-grants-2011_11