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Potassium Carbonate → 2-[4-[2-(imidazolo[4,5-b]pyridin-2-ylthio)ethyl]piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamide

HRID 1064871
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HRID 1064871 반응식
[SH:1][C:2]1[NH:3][C:4]2[C:5]([N:10]=1)=[N:6][CH:7]=[CH:8][CH:9]=2.C1OCCOCCOCCOCCOCCOC1.C(=O)([O-])[O-].[K+].[K+].CS(O[CH2:40][CH2:41][N:42]1[CH2:47][CH2:46][N:45]([CH2:48][C:49]([NH:51][C:52]2[C:53]([S:61][CH3:62])=[N:54][C:55]([CH3:60])=[CH:56][C:57]=2[S:58][CH3:59])=[O:50])[CH2:44][CH2:43]1)(=O)=O>CN(C=O)C.O>[NH:3]1[C:4]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[N:10]=[C:2]1[S:1][CH2:40][CH2:41][N:42]1[CH2:47][CH2:46][N:45]([CH2:48][C:49]([NH:51][C:52]2[C:53]([S:61][CH3:62])=[N:54][C:55]([CH3:60])=[CH:56][C:57]=2[S:58][CH3:59])=[O:50])[CH2:44][CH2:43]1
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참가 물질

7

반응물 4

HCID 11430Potassium CarbonateHCID 2855718-Crown-6HCID 22272586HCID 22272586, 화합물HCID 178527819HCID 178527819, 화합물

생성물 1

HCID 222727162-[4-[2-(imidazolo[4,5-b]pyridin-2-ylthio)ethyl]piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamide수율 40%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 6228Dimethylformamide용매2회

실험 절차

To a solution of 2-mercaptoimidazolo[4,5-b]pyridine (38.1 mg, 0.252 mmol) in DMF (0.5 ml) were added 18-crown-6 (6.6 mg, 0.025 mmol) and potassium carbonate (63 mg, 0.454 mmol) and the mixture was stirred. Then to the mixture was dropped a solution of crude 2-[4-(2-methanesulfonyloxyethyl)piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamide in DMF (1 ml) and stirred at 80° C. for 2 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and a saturated sodium chloride solution successively, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting residue was purified by a silica gel preparative thin layer chromatography (developing solvent; chloroform:methanol=10:1) to provide 51 mg (yield 40%) of the desired compound as colorless powdery crystals. IR (KBr) cm−1: 3140, 1688, 1600, 1564, 1485. 1H-NMR (CDCl3) δ: 2.38 (3H, s), 2.46 (3H, s), 2.49 (3H, s), 2.72-3.00 (10H, m), 3.29 (2H, s), 3.37 (2H, t, J=5.8 Hz), 6.63 (1H, s), 7.12 (1H, dd. J=7.8, 4.9 Hz), 7.82 (1H, d. J=7.8 Hz), 8.25 (1H, d. J=4.9 Hz), 8.49 (1H, br s).

후처리

  1. stirringstirred at 80° C. for 2 hours
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materiala saturated sodium chloride solution successively, dried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe resulting residue was purified by a silica gel preparative thin layer chromatography (developing solvent; chloroform:methanol=10:1)

출처 및 근거

ORD 기록
ord-d5fe4e1cbfed47168fb406c3d23e7dfe
출처 데이터셋
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06969711B2

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