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2-Methoxyethylamine → 5-Chloro-6-[(2-methoxyethyl)amino]nicotinonitrile

HRID 1631008
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HRID 1631008 반응식
[CH3:1][O:2][CH2:3][CH2:4][NH2:5].[Cl:6][C:7]1[C:8](Cl)=[N:9][CH:10]=[C:11]([CH:14]=1)[C:12]#[N:13]>O1CCOCC1>[Cl:6][C:7]1[C:8]([NH:5][CH2:4][CH2:3][O:2][CH3:1])=[N:9][CH:10]=[C:11]([CH:14]=1)[C:12]#[N:13]
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참가 물질

4

반응물 2

HCID 80182-MethoxyethylamineHCID 128784645,6-Dichloropyridine-3-carbonitrile

생성물 1

HCID 585542235-Chloro-6-[(2-methoxyethyl)amino]nicotinonitrile

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A mixture of 2-methoxyethyl amine (4.11 mL, 43.9 mmol), TEA (6.11 mL, 43.9 mmol) and 5,6-dichloronicotinonitrile (Bionet GC-0755, 7.6 g, 43.9 mmol) was prepared in dioxane and stirred at RT for 24 hours. The reaction mixture was filtered to remove inorganic solids and filtrate was concentrated under reduced pressure. The residue taken up with EtOAc (100 mL) and washed with water (3×100 mL). The organic layer was dried (Na2SO4) and concentrated under reduced pressure. After purification by flash chromatography (silica, pet ether/EtOAc), the title compound was obtained as a white powder (6.9 g, 75%). LC/MS, M+(ESI): 212.1. 1H NMR (DMSO-d6, 400 MHz) δ 8.42 (1H, d), 8.07 (1H, d), 7.48 (1H, t), 3.58 (2H, m), 3.47 (2H, m), 3.23 (3H, s).

후처리

  1. filtrationThe reaction mixture was filtered
  2. customto remove inorganic solids and filtrate
  3. concentrationwas concentrated under reduced pressure
  4. washwashed with water (3×100 mL)
  5. dry with materialThe organic layer was dried (Na2SO4)
  6. concentrationconcentrated under reduced pressure
  7. customAfter purification by flash chromatography (silica, pet ether/EtOAc)

출처 및 근거

ORD 기록
ord-417ddcd8f6e84a2baffa3d5d98a160f8
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08791142B2

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