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Methyl iodide → HCID 20751408, 화합물

HRID 2238631
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HRID 2238631 반응식
CN(C)/[CH:3]=[CH:4]/[C:5]([C:7]1[N:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]2=[N:9][CH:8]=1)=O.[NH2:17][C:18]([NH2:20])=[S:19].[CH3:21][O-].[Na+].CI>C(O)CCC>[CH3:21][S:19][C:18]1[N:20]=[C:5]([C:7]2[N:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]3=[N:9][CH:8]=2)[CH:4]=[CH:3][N:17]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6328Methyl iodideHCID 2723790ThioureaHCID 10942334Sodium MethoxideHCID 59176797HCID 59176797, 화합물

생성물 1

HCID 20751408HCID 20751408, 화합물수율 64.7%

시약·촉매·용매 1

HCID 2631-Butanol용매

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온도
85 °C

실험 절차

1 g of (E)-3-(dimethylamino)-1-imidazo[1,2-a]pyridin-3-yl-2-propen-1-one [1-2] was dissolved in 10 mL of n-butanol, then 354 mg of thiourea and 377 mg of sodium methoxide were added, and the mixture was stirred at 85° C. for 2 hours. After cooling back to the room temperature, 868 μL of methyl iodide was added, and stirred at room temperature for 30 minutes. The solvent was distilled off until the volume is halved, the solid thus produced was taken and washed with diethyl ether and with water in the subsequent order, and then dried under reduced pressure to obtain 728 mg of 3-[2-methylthio-4-pyrimidinyl]imidazo[1,2-a]pyridine [1-3] as a grey solid.

후처리

  1. additionwas added
  2. stirringstirred at room temperature for 30 minutes
  3. distillationThe solvent was distilled off until the volume
  4. customthe solid thus produced
  5. washwashed with diethyl ether and with water in the subsequent order
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-df210168c0fb47bfb2c8f3e98cc495e8
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07718801B2

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