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

HRID 2194161
ノート
印刷プレビュー

反応式

HRID 2194161 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 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

生成物 1

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

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

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+)

後処理

  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)

出典と根拠

ORDレコード
ord-6e83412157404509addf6af05e72eb1e
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08329904B2

反応ノート

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