Methyl Isocyanate → 5-[2-(Methylcarbamoylamino)ethylthio]imidazo[1,2-a]pyridine

HRID 1081716

반응식

HRID 1081716 반응식
[NH2:1][CH2:2][CH2:3][S:4][C:5]1[N:10]2[CH:11]=[CH:12][N:13]=[C:9]2[CH:8]=[CH:7][CH:6]=1.[CH3:14][N:15]=[C:16]=[O:17]>C(Cl)Cl>[CH3:14][NH:15][C:16]([NH:1][CH2:2][CH2:3][S:4][C:5]1[N:10]2[CH:11]=[CH:12][N:13]=[C:9]2[CH:8]=[CH:7][CH:6]=1)=[O:17]

참가 물질

4

반응물 2

HCID 12228Methyl IsocyanateHCID 152293695-[2-(Amino)ethylthio]imidazo[1,2-a]pyridine

생성물 1

HCID 539413315-[2-(Methylcarbamoylamino)ethylthio]imidazo[1,2-a]pyridine수율 86%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (1.93 g, 10 moles) in methylene chloride (30 ml) was added methyl isocyanate (0.59 ml, 10 moles) under ice-cooling with stirring and the mixture was stirred under ice-cooling for 1 hour. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:5) to obtain 2.15 g of the desired product (86.0%, pale yellow crystals).

후처리

  1. temperaturecooling
  2. stirringthe mixture was stirred under ice-
  3. temperaturecooling for 1 hour
  4. distillationAfter the solvent was distilled off
  5. customthe residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:5)

출처 및 근거

ORD 기록
ord-2f8b420523be410ea0e2facc2ae2bd2f
출처 데이터셋
uspto-grants-1996_12
특허 번호
US05587383

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