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Methyl iodide → N-(2,4-dichloro-thiazol-5-yl)-N-methyl-3-methylsulfanyl-propionamide

HRID 533338
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HRID 533338 반응식
[Cl:1][C:2]1[S:3][C:4]([NH:8][C:9](=[O:14])[CH2:10][CH2:11][S:12][CH3:13])=[C:5]([Cl:7])[N:6]=1.[C:15]([O-])([O-])=O.[K+].[K+].IC>CN(C=O)C.O>[Cl:1][C:2]1[S:3][C:4]([N:8]([CH3:15])[C:9](=[O:14])[CH2:10][CH2:11][S:12][CH3:13])=[C:5]([Cl:7])[N:6]=1
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참가 물질

6

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 59580948N-(2,4-dichloro-thiazol-5-yl)-3-methylsulfanyl-propionamide

생성물 1

HCID 59580788N-(2,4-dichloro-thiazol-5-yl)-N-methyl-3-methylsulfanyl-propionamide수율 44%

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매

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온도
25 °C

실험 절차

To a solution of N-(2,4-dichloro-thiazol-5-yl)-3-methylsulfanyl-propionamide (596 mg, 2.2 mmol) in DMF (11 mL) stiffing at 25° C. was added K2CO3 (365 mg, 2.64 mmol) and iodomethane (375 mg, 1.2 mmol), the solution was stirred at 25° C. for 20 h. The solution was diluted with 50 mL H2O and extracted with ethyl acetate (3×20 mL). The combined organic extracts were washed with H2O (3×20 mL), dried over Na2SO4, filtered and concentrated to dryness under reduced pressure. The crude product was purified by silica gel chromatography (0 to 100% ethyl acetate/hexanes) to give the desired product as a clear oil (273 mg, 44%): 1H NMR (300 MHz, CDCl3) δ 3.23 (s, 3H), 2.79 (t, J=7.2 Hz, 2H), 2.52 (t, J=7.2 Hz, 2H), 2.09 (s, 3H); ESIMS m/z 285.1 (M+1).

후처리

  1. customstiffing at 25° C.
  2. extractionextracted with ethyl acetate (3×20 mL)
  3. washThe combined organic extracts were washed with H2O (3×20 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated to dryness under reduced pressure
  7. customThe crude product was purified by silica gel chromatography (0 to 100% ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-11f9dc07b6fe40789955360bf0e12d15
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853246B2

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