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Sodium Iodide → 5-Iodo-3-(trifluoromethyl)pyridin-2-amine

HRID 268965
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HRID 268965 반응식
Br[C:2]1[CH:3]=[C:4]([C:9]([F:12])([F:11])[F:10])[C:5]([NH2:8])=[N:6][CH:7]=1.[I-:13].[Na+]>C(O)CCC.[Cu]I.CNCCNC>[I:13][C:2]1[CH:3]=[C:4]([C:9]([F:12])([F:11])[F:10])[C:5]([NH2:8])=[N:6][CH:7]=1
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참가 물질

6

반응물 2

HCID 5238Sodium IodideHCID 205253835-Bromo-3-(trifluoromethyl)pyridin-2-amine

생성물 1

HCID 582353065-Iodo-3-(trifluoromethyl)pyridin-2-amine수율 102%

시약·촉매·용매 3

HCID 8070N,N'-Dimethylethylenediamine촉매HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매

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온도
23 °C

실험 절차

A mixture of 5-bromo-3-trifluoromethyl-pyridin-2-ylamine (example C.18 step 3) (723 mg, 3 mmol), sodium iodide (900 mg, 6 mmol), copper (I) iodide (29 mg, 5 mol %) and N,N′-dimethylethylendiamine (26 mg, 10 mol %) in n-butanol (6 mL) was stirred at reflux under argon atmosphere for 18 h. The reaction mixture was cooled to 23° C., extracted with ethyl acetate and water, the organic layers were dried over MgSO4, filtered and evaporated to leave the title compound as a brown solid (880 mg, 102%), which was used without further purification. MS (ISN) 287.0 [(M−H)−].

후처리

  1. temperatureat reflux under argon atmosphere for 18 h
  2. extractionextracted with ethyl acetate and water
  3. dry with materialthe organic layers were dried over MgSO4
  4. filtrationfiltered
  5. customevaporated

출처 및 근거

ORD 기록
ord-a774a02f03634853adede33f69fc3246
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07446113B2

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HCID 263
1-Butanol
용매