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Sodium Thiosulfate → 2-Chloro-3-(1-fluorocyclobutyl)-6-methylpyridine 1-oxide

HRID 624993
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HRID 624993 반응식
ClC1C=C(C=CC=1)C(OO)=[O:6].[Cl:12][C:13]1[C:18]([C:19]2([F:23])[CH2:22][CH2:21][CH2:20]2)=[CH:17][CH:16]=[C:15]([CH3:24])[N:14]=1.[O-]S([O-])(=S)=O.[Na+].[Na+]>ClCCl>[Cl:12][C:13]1[C:18]([C:19]2([F:23])[CH2:22][CH2:21][CH2:20]2)=[CH:17][CH:16]=[C:15]([CH3:24])[N+:14]=1[O-:6]
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참가 물질

5

반응물 3

HCID 24477Sodium ThiosulfateHCID 70297m-Chloroperbenzoic acidHCID 902024992-Chloro-3-(1-fluorocyclobutyl)-6-methylpyridine

생성물 1

HCID 902025652-Chloro-3-(1-fluorocyclobutyl)-6-methylpyridine 1-oxide수율 75%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

3-Chlorobenzoperoxoic acid (173 mg, 1.00 mmol) was added in 2 portions to a solution of 2-chloro-3-(1-fluorocyclobutyl)-6-methylpyridine (Example 130 b, 100 mg, 501 μmol) in dichloromethane (2 mL). The reaction mixture was stirred at ambient temperature for 72 h, poured onto a 10% aqueous Na2S2O3 solution (30 mL) and extracted with dichloromethane (2×40 mL). The combined organic layers were washed with ice water/brine (30 mL), dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in dichloromethane, washed with sat. NaHCO3 solution (30 mL) and ice water (30 mL), dried over Na2SO4 and concentrated in vacuo to give the title compound (81 mg, 74%) as yellow oil, MS (ESI): m/e=216.3 [MH+].

후처리

  1. extractionextracted with dichloromethane (2×40 mL)
  2. washThe combined organic layers were washed with ice water/brine (30 mL)
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. dissolutionThe residue was dissolved in dichloromethane
  6. washwashed with sat. NaHCO3 solution (30 mL) and ice water (30 mL)
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9e6f35e3eddb4e7cb0b3b8c060ba9254
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09303012B2

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