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N-Iodosuccinimide → Methyl 3-iodoimidazo[1,2-a]pyridine-8-carboxylate

HRID 1423032
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HRID 1423032 반응식
[CH3:1][O:2][C:3]([C:5]1[C:6]2[N:7]([CH:11]=[CH:12][N:13]=2)[CH:8]=[CH:9][CH:10]=1)=[O:4].[I:14]N1C(=O)CCC1=O>C(#N)C>[CH3:1][O:2][C:3]([C:5]1[C:6]2[N:7]([C:11]([I:14])=[CH:12][N:13]=2)[CH:8]=[CH:9][CH:10]=1)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 15098894Methyl imidazo[1,2-a]pyridine-8-carboxylate

생성물 1

HCID 57355257Methyl 3-iodoimidazo[1,2-a]pyridine-8-carboxylate

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of imidazo[1,2-a]pyridine-8-carboxylic acid methyl ester (3.24 g, 18.3 mmol) and N-iodosuccinimide (NIS) (4.11 g, 18.3 mmol) in acetonitrile (50 mL) is stirred at room temperature. After 2 hours, the reaction mixture is quenched with saturated aqueous Na2S2O3 and extracted with EtOAc (3×100 mL). The combined organic layers are washed with water, brine, dried over Na2SO4 and concentrated. The crude material is purified by silica gel chromatography eluting with 80% EtOAc in hexanes to afford 3-iodo-imidazo[1,2-a]pyridine-8-carboxylic acid methyl ester. Mp: 99-110° C.

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후처리

  1. customthe reaction mixture is quenched with saturated aqueous Na2S2O3
  2. extractionextracted with EtOAc (3×100 mL)
  3. washThe combined organic layers are washed with water, brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated
  6. customThe crude material is purified by silica gel chromatography
  7. washeluting with 80% EtOAc in hexanes

출처 및 근거

ORD 기록
ord-5b7a530dc3364f0f8d5374c20e24666e
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927550B2

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