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Hydrochloric Acid → 6-[5-(2-Hydroxy-ethylamino)-pyridin-3-yl]-1-methyl-3,4-dihydro-1H-quinolin-2-one

HRID 1774787
ノート
印刷プレビュー

反応式

HRID 1774787 の反応式
C([Si](C)(C)[O:6][CH2:7][CH2:8][NH:9][C:10]1[CH:11]=[C:12]([C:16]2[CH:17]=[C:18]3[C:23](=[CH:24][CH:25]=2)[N:22]([CH3:26])[C:21](=[O:27])[CH2:20][CH2:19]3)[CH:13]=[N:14][CH:15]=1)(C)(C)C.Cl.O1CCOCC1>CO>[OH:6][CH2:7][CH2:8][NH:9][C:10]1[CH:11]=[C:12]([C:16]2[CH:17]=[C:18]3[C:23](=[CH:24][CH:25]=2)[N:22]([CH3:26])[C:21](=[O:27])[CH2:20][CH2:19]3)[CH:13]=[N:14][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 866791516-{5-[2-(tert-Butyl-dimethyl-silanyloxy)-ethylamino]-pyridin-3-yl}-1-methyl-3,4-dihydro-1H-quinolin-2-one

生成物 1

HCID 715331996-[5-(2-Hydroxy-ethylamino)-pyridin-3-yl]-1-methyl-3,4-dihydro-1H-quinolin-2-one収率 23%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To solution of 6-{5-[2-(tert-butyl-dimethyl-silanyloxy)-ethylamino]-pyridin-3-yl}-1-methyl-3,4-dihydro-1H-quinolin-2-one (0.06 g, 0.146 mmol) in MeOH (2.5 mL) was added 4M HCl in dioxane (0.255 ml, 1.02 mmol) and the reaction mixture was stirred at room temperature for 2 h. The mixture was concentrated in vacuo, the residue dissolved in EtOAc (20 mL) and washed with aq. NaHCO3 (5 mL). The organic layer was washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by silica gel flash chromatography eluting with a 0 to 2% MeOH(1% NH4OH)-DCM gradient to give the title compound (0.01 g, 22%) as an off white solid. MS: 298.3 (M+H+).

後処理

  1. concentrationThe mixture was concentrated in vacuo
  2. dissolutionthe residue dissolved in EtOAc (20 mL)
  3. washwashed with aq. NaHCO3 (5 mL)
  4. washThe organic layer was washed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. customevaporated to dryness
  8. customThe residue was purified by silica gel flash chromatography
  9. washeluting with a 0 to 2% MeOH(1% NH4OH)-DCM gradient

出典と根拠

ORDレコード
ord-a8b0723358504177b07681e78dac899d
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09260408B2

反応ノート

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