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

HRID 1625987
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HRID 1625987 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-d0c314362db740fca60b7e1eab165bfd
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08785438B2

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