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Sodium methanethiolate → 5-Bromo-2-methylsulfanylmethyl-pyridine

HRID 1484411
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HRID 1484411 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8]Cl)=[N:6][CH:7]=1.[CH3:10][S-:11].[Na+]>CN(C=O)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][S:11][CH3:10])=[N:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 4378561Sodium methanethiolateHCID 114015015-bromo-2-(chloromethyl)pyridine

생성물 1

HCID 1156223545-Bromo-2-methylsulfanylmethyl-pyridine수율 81%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

To the stirred solution of 5-Bromo-2-chloromethyl-pyridine (3.5 gm, 16.99 mmol) in DMF (25 mL) at 0° C. is added Sodium thiomethoxide (1.31 gm, 18.68 mmol) resulting reaction mixture is stirred at 0° C. for 2 h. After completion quenched with water and extracted with ethyl acetate (3×100 mL). The Combined organic layer is washed with brine and organic layer dried over sodium sulphate, evaporate under reduced pressure. The crude is purified by column chromatography using silica 100-200 mesh using 10% EtOAc: Hexane as eluent to afford title compound (3 g) as brown colored liquid. 1NMR (400 MHz, DMSO) δ: 2.00 (s, 3H), 3.75 (s, 2H), 7.39 (d, J=8.32 Hz, 1H), 7.99-8.02 (dd, J1=2.44 Hz, J2=8.32 Hz, 1H), 8.60 (d, J=2.28 Hz, 1H). LC-MS (m/z): M+H=220.1.

후처리

  1. customresulting
  2. customreaction mixture
  3. customAfter completion quenched with water
  4. extractionextracted with ethyl acetate (3×100 mL)
  5. washThe Combined organic layer is washed with brine and organic layer
  6. dry with materialdried over sodium sulphate
  7. customevaporate under reduced pressure
  8. customThe crude is purified by column chromatography

출처 및 근거

ORD 기록
ord-d131c5f4e7c041d196a4c2ed5a1a6949
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09422236B2

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