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Ammonia → 5-Bromo-3-iodo-4-methylpyridin-2-amine

HRID 2088952
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HRID 2088952 반응식
[Br:1][C:2]1[C:3]([CH3:9])=[CH:4][C:5]([NH2:8])=[N:6][CH:7]=1.[I:10]N1C(=O)CCC1=O.FC(F)(F)C(O)=O.N>C(O)(=O)C>[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([I:10])[C:5]([NH2:8])=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 222AmmoniaHCID 6422Trifluoroacetic acidHCID 120273N-IodosuccinimideHCID 8176952-Amino-5-bromo-4-methylpyridine

생성물 1

HCID 401518975-Bromo-3-iodo-4-methylpyridin-2-amine수율 94.5%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

5-Bromo-4-methylpyridine-2-amine (3.1 g) was dissolved in acetic acid (20 ml). N-Iodosuccinimide (3.8 g) and trifluoroacetic acid (0.2 ml) were added and the mixture was stirred at room temperature for 2.5 hours. The reaction solution was poured into ice water and neutralized with 28% aqueous ammonia. Then, the precipitated solid was collected by filtration, washed with water and dried to give the title compound (4.9 g).

후처리

  1. filtrationThen, the precipitated solid was collected by filtration
  2. washwashed with water
  3. customdried

출처 및 근거

ORD 기록
ord-828b4177bc2d4c569dad569a1bb7cb65
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08436012B2

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