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Sodium Carbonate → HCID 90389673, 화합물

HRID 59765
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HRID 59765 반응식
[I:1][C:2]1[C:3](N)=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH3:9].[H+].[B-](F)(F)(F)[F:13].N([O-])=O.[Na+].C([O-])([O-])=O.[Na+].[Na+]>O>[F:13][C:3]1[C:2]([I:1])=[C:7]([O:8][CH3:9])[CH:6]=[CH:5][N:4]=1
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참가 물질

6

반응물 4

HCID 10340Sodium CarbonateHCID 28118Tetrafluoroboric acidHCID 23668193Sodium NitriteHCID 242292063-Iodo-4-methoxypyridin-2-amine

생성물 1

HCID 90389673HCID 90389673, 화합물

시약·촉매·용매 1

HCID 962Water용매

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온도
-20 °C

실험 절차

To a cold (−20° C.), stirred suspension of the 3-iodo-4-methoxypyridin-2-amine (2.5 g, 10 mmol) in HBF4 (70 mL, 470 mmol) was added an aqueous solution of NaNO2 (1.67 M, 6 mL, 10 mmol) over 20 min. The reaction turned green and then brown in color. The mixture was stirred at 0° C. for 3 h. The reaction was then carefully poured into a cold (0° C.) saturated solution of Na2CO3 (50 g) in H2O (100 mL). The layer was then extracted with EtOAc (×3). The combined organic layers were dried over anhydrous MgSO4, filtered, and concentrated under vacuum to leave a residue which was purified by column chromatography on silica gel (elution with 5:1 to 2:1 hexanes:ethyl acetate) to yield 2-fluoro-3-iodo-4-methoxypyridine as a light yellow solid.

후처리

  1. stirringThe mixture was stirred at 0° C. for 3 h
  2. extractionThe layer was then extracted with EtOAc (×3)
  3. dry with materialThe combined organic layers were dried over anhydrous MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum
  6. customto leave a residue which
  7. customwas purified by column chromatography on silica gel (elution with 5:1 to 2:1 hexanes:ethyl acetate)

출처 및 근거

ORD 기록
ord-940df2b609564ca49e67ea9a7eb5af63
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09440952B2

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