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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 887701생성일: 2026년 10월 25일

Triethylamine → 6,8-dichloro-2-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-pyrido[3,4-d][1,3]oxazin-4-one

https://huagongshe.com/reaction/887701

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl ChlorideHCID 18446928—
반응물3-Amino-2,6-dichloroisonicotinic acidHCID 59355521—
용매AcetonitrileHCID 6342—
생성물6,8-dichloro-2-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-pyrido[3,4-d][1,3]oxazin-4-oneHCID 5935552496.9%

반응 단계

5-Trifluoromethyl-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid chloride (example 2, step 3) (242 mg) was added to a mixture of 3-amino-2,6-dichloroisonicotinic acid (example 1, step 8) (190 mg) in acetonitrile (3 mL). The mixture was stirred for 5 minutes at room temperature and triethylamine (220 μL) was added and stirred for 20 minutes, before a second portion of triethylamine (220 μL) was added. After the mixture was stirred for further 20 minutes at room temperature, methanesulfonyl chloride (70 μL) was added. After stirring for 2 hours at room temperature, the formed precipitate was filtered off, washed carefully with water and MTB-ether and dried in vacuum to afford 350 mg of the title compound of the formula

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247431B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-656341aedc0b496abd1d564216721c1d
출처 메모uspto-grants-2012_08