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1,3,5-trimethyl-1H-pyrazole-4-sulfonyl chloride → 2,8-Diazaspiro(4.5)decan-1-one

HRID 2194161
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HRID 2194161 반응식
C(O)(=O)C.FC(F)(F)OC1C=CC([N:14]2[CH2:18][CH2:17][C:16]3([CH2:23][CH2:22][NH:21][CH2:20][CH2:19]3)[C:15]2=[O:24])=CC=1.CN1C(C)=C(S(Cl)(=O)=O)C(C)=N1>N1C=CC=CC=1>[C:15]1(=[O:24])[C:16]2([CH2:23][CH2:22][NH:21][CH2:20][CH2:19]2)[CH2:17][CH2:18][NH:14]1
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참가 물질

4

반응물 2

HCID 27373401,3,5-trimethyl-1H-pyrazole-4-sulfonyl chlorideHCID 667873332-(4-Trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one acetic acid salt

생성물 1

HCID 222250112,8-Diazaspiro(4.5)decan-1-one수율 1,167.2%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

2-(4-Trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one acetic acid salt (0.02 g, 0.05 mmol) was dissolved in pyridine (0.5 ml) at room temperature and 1,3,5-trimethyl-1H-pyrazole-4-sulfonyl chloride (0.013 g, 0.06 mmol) was added and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated in vacuo and the resulting residue was dissolved in AcOEt and washed with 0.1M HCl and brine. The organic layer was dried (Na2SO4), filtered and evaporated under reduced pressure to give a crude residue which was purified by flash column chromatography (4:1 AcOEt/heptane) to yield 2-(4-trifluoromethoxy-phenyl)-8-(1,3,5-trimethyl-1H-pyrazole-4-sulfonyl)-2,8-diaza-spiro[4.5]decan-1-onel)-2,8-diaza-spiro[4.5]decan-1-one as an off-white solid (0.09 g, 31%). MS (ESI): 487.3 (MH+)

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. dissolutionthe resulting residue was dissolved in AcOEt
  3. washwashed with 0.1M HCl and brine
  4. dry with materialThe organic layer was dried (Na2SO4)
  5. filtrationfiltered
  6. customevaporated under reduced pressure
  7. customto give a crude residue which
  8. customwas purified by flash column chromatography (4:1 AcOEt/heptane)

출처 및 근거

ORD 기록
ord-6e83412157404509addf6af05e72eb1e
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08329904B2

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