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Pyridine → HCID 18466614, 화합물

HRID 2229329
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HRID 2229329 반응식
[NH2:1][C:2]1[C:3]([Cl:10])=[N:4][C:5]([Cl:9])=[CH:6][C:7]=1[CH3:8].N1C=CC=CC=1.[Br:17][C:18]1[CH:19]=[C:20]([C:25](Cl)=[O:26])[C:21]([Cl:24])=[N:22][CH:23]=1>C1(C)C=CC=CC=1.O>[Br:17][C:18]1[CH:19]=[C:20]([C:25]([NH:1][C:2]2[C:3]([Cl:10])=[N:4][C:5]([Cl:9])=[CH:6][C:7]=2[CH3:8])=[O:26])[C:21]([Cl:24])=[N:22][CH:23]=1
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참가 물질

6

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HCID 1049PyridineHCID 7010123-Amino-2,6-dichloro-4-methylpyridineHCID 126772955-Bromo-2-chloro-3-pyridinecarbonyl chloride

생성물 1

HCID 18466614HCID 18466614, 화합물수율 36.4%

시약·촉매·용매 2

HCID 962Water용매HCID 1140Toluene용매

실험 절차

3-Amino-2,6-dichloro-4-methylpyridine (0.51 g, 2.85 mmol) was dissolved in toluene (35 mL) and pyridine (0.27 mL, 3.28 mmol) was added. 5-Bromo-2-chloro-3-pyridinecarbonyl chloride (0.80 g, 3.14 mmol) was then added dropwise over 30 min. The resulting mixture was stirred at room temperature for 1 h, diluted with water and extracted with toluene (2×). The combined organic extracts were dried (MgSO4), filtered and concentrated under reduced pressure. The resulting thick oil was triturated with CH2Cl2, and the white solid collected via suction filtration to give the title compound (0.41 g, 36% yield).

후처리

  1. extractionextracted with toluene (2×)
  2. dry with materialThe combined organic extracts were dried (MgSO4)
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe resulting thick oil was triturated with CH2Cl2
  6. filtrationthe white solid collected via suction filtration

출처 및 근거

ORD 기록
ord-63adb8d9fd6842fba6fc6fa6b267b8e0
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06420359B1

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