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Hydrogen Bromide → HCID 67399727, 화합물

HRID 70708
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HRID 70708 반응식
Br.[CH:2]1([S:5][C:6]2[CH:11]=[CH:10][C:9]([C:12]([C:14]3[CH:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[C:16]([O:24]C)[N:15]=3)=[O:13])=[CH:8][CH:7]=2)[CH2:4][CH2:3]1.O>O1CCOCC1>[CH:2]1([S:5][C:6]2[CH:7]=[CH:8][C:9]([C:12]([C:14]3[NH:15][C:16](=[O:24])[C:17]([C:20]([F:23])([F:22])[F:21])=[CH:18][CH:19]=3)=[O:13])=[CH:10][CH:11]=2)[CH2:4][CH2:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 260Hydrogen BromideHCID 962WaterHCID 58452661HCID 58452661, 화합물

생성물 1

HCID 67399727HCID 67399727, 화합물수율 55%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
65 °C

실험 절차

48% hydrobromic acid (2 mL) was added to a solution of [4-(cyclopropylsulfanyl)phenyl][6-methoxy-5-(trifluoromethyl)pyridin-2-yl]methanone obtained in Reference Example 1-68 (400 mg) in 1,4-dioxane (4 mL), and the mixture was stirred at 65° C. for one hour. Water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1→1:5) to give 6-{[4-(cyclopropylsulfanyl)phenyl]carbonyl}-3-(trifluoromethyl)pyridin-2(1H)-one (210 mg, 55%).

후처리

  1. extractionfollowed by extraction with ethyl acetate
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. customafter which the solvent was evaporated under reduced pressure
  4. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1→1:5)

출처 및 근거

ORD 기록
ord-07d6a2cdde0b459fabe3aa3c515e4a1d
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822503B2

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