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N-Iodosuccinimide → 7-Bromo-3-chloro-8-iodoisoquinoline

HRID 1465751
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반응식

HRID 1465751 반응식
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[C:7]([Cl:12])[N:8]=[CH:9]2)=[CH:4][CH:3]=1.C1C(=O)N([I:20])C(=O)C1>S(O)(C(F)(F)F)(=O)=O>[Br:1][C:2]1[C:11]([I:20])=[C:10]2[C:5]([CH:6]=[C:7]([Cl:12])[N:8]=[CH:9]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 513419807-Bromo-3-chloroisoquinoline

생성물 1

HCID 895252237-Bromo-3-chloro-8-iodoisoquinoline

시약·촉매·용매 1

HCID 62406Trifluoromethanesulfonic acid용매

실험 절차

To a flask containing 7-Bromo-3-chloroisoquinoline (1.5 g, 6.19 mmol) was added NIS (1.4 g, 6.9 mmol). The flask was placed in an ice bath and treated with TfOH (40 mL) and stirred at RT overnight. The reaction mixture was carefully poured into ice, and the aqueous layer was extracted with DCM. The combined extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The crude residue was purified by silica gel column chromatography (Hexanes:DCM→1:1) to provide the title product.

후처리

  1. customThe flask was placed in an ice bath
  2. additionThe reaction mixture was carefully poured into ice
  3. extractionthe aqueous layer was extracted with DCM
  4. washThe combined extracts were washed with brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. customThe crude residue was purified by silica gel column chromatography (Hexanes:DCM→1:1)

출처 및 근거

ORD 기록
ord-ed496408991d4f62b8fd0a4513bf584d
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999991B2

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