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Hydride → 8-Fluoroquinolin-4-amine

HRID 1608946
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HRID 1608946 반응식
[N:1]([C:4]1[C:13]2[C:8](=[C:9]([F:14])[CH:10]=[CH:11][CH:12]=2)[N:7]=[CH:6][CH:5]=1)=[N+]=[N-].[BH4-].[Na+].[H-]>C(O)C>[NH2:1][C:4]1[C:13]2[C:8](=[C:9]([F:14])[CH:10]=[CH:11][CH:12]=2)[N:7]=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 166653HydrideHCID 4311764Sodium borohydrideHCID 157905214-Azido-8-fluoroquinoline

생성물 1

HCID 157905048-Fluoroquinolin-4-amine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution at 15°-20° C. of 4-azido-8-fluoroquinoline in 12 mL of absolute ethanol was added a portion of 0.57 g (0.015 mol) of sodium borohydride. A powerful exotherm with vigorous evolution of gas was observed. The solution was cooled in ice and the remainder of the hydride was added in small portions within five minutes. The ice bath was then removed. After about two hours, the mixture was poured into about 200 mL of ice water. The precipitate was collected and air dried overnight. Yield 1.35 g. M.P. 184°-186° C.

후처리

  1. temperatureThe solution was cooled in ice
  2. customThe ice bath was then removed
  3. additionthe mixture was poured into about 200 mL of ice water
  4. customThe precipitate was collected
  5. customair dried overnight

출처 및 근거

ORD 기록
ord-270b9ec410a841399158ea7ee3967c68
출처 데이터셋
uspto-grants-1995_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05399564

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