Ethyl Acetate → 2-(3-ethynyl-quinolin-6-yloxy)-N-(1-hydroxymethyl-1-methylprop-2-ynyl)-2-methylsulfanyl acetamide

HRID 1892053ノート

反応式

HRID 1892053 の反応式
[F-].C([N+](CCCC)(CCCC)CCCC)CCC.C([SiH2][O:24][C:25](C1C=CC=CC=1)(C1C=CC=CC=1)[C:26]([NH:30][C:31](=[O:48])[CH:32]([O:35][C:36]1[CH:37]=[C:38]2[C:43](=[CH:44][CH:45]=1)[N:42]=[CH:41][C:40]([C:46]#[CH:47])=[CH:39]2)[S:33][CH3:34])([CH3:29])[C:27]#[CH:28])(C)(C)C.C(OCC)(=O)C>C1COCC1.[Cl-].[Na+].O>[C:46]([C:40]1[CH:41]=[N:42][C:43]2[C:38]([CH:39]=1)=[CH:37][C:36]([O:35][CH:32]([S:33][CH3:34])[C:31]([NH:30][C:26]([CH2:25][OH:24])([CH3:29])[C:27]#[CH:28])=[O:48])=[CH:45][CH:44]=2)#[CH:47]

参加物

6

反応物 3

HCID 8857Ethyl AcetateHCID 2724141Tetrabutylammonium FluorideHCID 178437010HCID 178437010、化合物

生成物 1

HCID 595653502-(3-ethynyl-quinolin-6-yloxy)-N-(1-hydroxymethyl-1-methylprop-2-ynyl)-2-methylsulfanyl acetamide収率 72.5%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 57417360Sodium chloride; water溶媒

実験手順

A solution of tetrabutylammonium fluoride (1 M) in THF was added dropwise to a solution of N-[1-(tert-butyl-diphenyl-silanyloxymethyl)-1-methyl-prop-2-ynyl]-2-(3-ethynyl-quinolin-6-yloxy)-2-methylsulfanyl-acetamide (1.49 g) at 0° C. The reaction mixture was allowed to warm up to room temperature, further stirred for 1 h 20 and then, poured onto a mixture of ethyl acetate and brine. The two layers were separated and the aqueous layer was extracted thrice with ethyl acetate. The organic layers were combined, washed once with brine and then dried over sodium sulphate. After filtration and concentration under reduced pressure 2.47 g of crude mixture were isolated as a yellow oil. The residue was purified by flash chromatography on silica gel (hexane/ethyl acetate) to give 0.646 g of 2-(3-Ethynyl-quinolin-6-yloxy)-N-(1-hydroxymethyl-1-methylprop-2-ynyl)-2-methylsulfanyl acetamide as a white solid (m.p.=150-150° C.).

後処理

  1. customThe two layers were separated
  2. extractionthe aqueous layer was extracted thrice with ethyl acetate
  3. washwashed once with brine
  4. dry with materialdried over sodium sulphate
  5. filtrationAfter filtration and concentration under reduced pressure 2.47 g of crude mixture
  6. customwere isolated as a yellow oil
  7. customThe residue was purified by flash chromatography on silica gel (hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-0f77c1fa4b734fea88993dec4b6f1c9c
出典データセット
uspto-grants-2013_08
特許番号
US08507509B2

反応ノート

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