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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 559805생성일: 2026년 10월 25일

Sodium Acetate → 5-(2-Amino-thiazol-4-yl)-6-methyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamide

https://huagongshe.com/reaction/559805

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AcetateHCID 517045—
반응물ThioureaHCID 2723790—
반응물5-(bromoacetyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamideHCID 86614780—
용매EthanolHCID 702—
생성물5-(2-Amino-thiazol-4-yl)-6-methyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamideHCID 8661478169%

반응 조건

온도90 °C

반응 단계

5-Bromoacetyl-6-methyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamide (Example 50 (c), 0.04 g, 0.067 mmol), thiourea (0.0067 g, 0.086 mmol), NaOAc (0.011 g, 0.136 mmol), EtOH (2 ml) and a magnetic stirrer bar were placed in a tube designed for microwave synthesis. The vial was sealed and the mixture was heated in a CEM Discover Microwave apparatus (100 W, 90° C.) for 20 minutes, giving complete conversion of the starting material to a single product according to LC-MS. The solvents were evaporated to give a crude mixture which was purified on preparative HPLC giving the title compound (0.026 g, 66%) as a slightly yellowish solid after freeze-drying the pure fractions.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063073B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-c592cdfe75d94b09a39bfd1a930bba25
출처 메모uspto-grants-2011_11