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Triethylamine → HCID 178458617, 화합물

HRID 75941
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HRID 75941 반응식
[F:1][C:2]1[N:9]=[C:8](F)[C:7]([F:11])=[CH:6][C:3]=1[C:4]#[N:5].C(N(CC)CC)C.[CH:19]([O:22][C:23]1[NH:27][N:26]=[C:25]([NH2:28])[CH:24]=1)([CH3:21])[CH3:20]>C(#N)C.O>[F:1][C:2]1[N:9]=[C:8]([NH:28][C:25]2[CH:24]=[C:23]([O:22][CH:19]([CH3:21])[CH3:20])[NH:27][N:26]=2)[C:7]([F:11])=[CH:6][C:3]=1[C:4]#[N:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

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HCID 8471TriethylamineHCID 404271652,5,6-TrifluoronicotinonitrileHCID 1784587215-Isopropoxy-1H-pyrazol-3-amine

생성물 1

HCID 178458617HCID 178458617, 화합물수율 9%

시약·촉매·용매 2

HCID 962Water용매HCID 6342Acetonitrile용매2회

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온도
0 °C

실험 절차

To a solution of 2,5,6-trifluoronicotinonitrile (3.0 g, 19.0 mmol) and triethylamine (2.5 g, 24.7 mmol) in ACN (30 ml) at 0° C. was added 5-isopropoxy-1H-pyrazol-3-amine (2.95 g, 20.9 mmol) in ACN (15 ml). The reaction was stirred at 0° C. for 1 hour, at which point the reaction was diluted with water (50 ml) and extracted with DCM (2×50 ml). The combined organic fractions were dried over Na2SO4, filtered, and then concentrated. The resulting oil was purified by column chromatography (DCM-MeOH=100:1) to give the title compound (0.48 g, 9%). MS: Calcd.: 279. Found: [M+H]+ 280.

후처리

  1. extractionextracted with DCM (2×50 ml)
  2. dry with materialThe combined organic fractions were dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe resulting oil was purified by column chromatography (DCM-MeOH=100:1)

출처 및 근거

ORD 기록
ord-34fe19abe51f4b648f367a2b04be5fb6
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835465B2

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