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Methyl iodide → 6-Chloro-5-iodo-2-(methylthio)-1H-imidazo[4,5-b]pyridine

HRID 1050256
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HRID 1050256 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[NH:11][C:10](=[S:12])[NH:9][C:5]2=[N:6][C:7]=1[I:8].[OH-].[K+].I[CH3:16]>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]2[NH:11][C:10]([S:12][CH3:16])=[N:9][C:5]2=[N:6][C:7]=1[I:8]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 14797Potassium HydroxideHCID 866847396-Chloro-5-iodo-1H-imidazo[4,5-b]pyridine-2(3H)-thione

생성물 1

HCID 895582656-Chloro-5-iodo-2-(methylthio)-1H-imidazo[4,5-b]pyridine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of 6-chloro-5-iodo-1,3-dihydro-2H-imidazo[4,5-b]pyridine-2-thione (11.0 g, 35.3 mmol) and KOH (2.38 g, 42.4 mmol) in ethanol (200 mL) was stirred at rt for 0.5 h. Iodomethane (2.2 mL, 35.3 mmol) was then added and the reaction was allowed to stir for 1 h at rt. The ethanol was removed in vacuo and the resulting residue was partitioned between ethyl acetate (250 mL) and 2N HCl (50 mL). The ethyl acetate layer was washed with brine, dried over magnesium sulfate, filtered through a 100 g pad of silica gel and concentrated to give the desired product as a white solid. LC-MS: calculated for C7H5ClIN3S 325.56, observed m/e: 325.88 (M+H)+ (Rt 2.05/5 min).

후처리

  1. stirringto stir for 1 h at rt
  2. customThe ethanol was removed in vacuo
  3. customthe resulting residue was partitioned between ethyl acetate (250 mL) and 2N HCl (50 mL)
  4. washThe ethyl acetate layer was washed with brine
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered through a 100 g pad of silica gel
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f005345b921f448baad35dfa87d24d9f
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09382243B2

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