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Phosphorus oxychloride → 1-(4-cyanophenyl)-5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl)-1H-pyrazole-4-sulfonamide

HRID 576800
ノート
印刷プレビュー

反応式

HRID 576800 の反応式
C([NH:8][C@H]1CCCC[C@H]1CO)C1C=CC=CC=1.[C:17]([C:19]1[CH:24]=[CH:23][C:22]([N:25]2[C:29]([C:30]3[C:31](=[O:49])[N:32]([CH3:48])[C:33](=[O:47])[N:34]([C:37]4[CH:42]=[CH:41][CH:40]=[C:39]([C:43]([F:46])([F:45])[F:44])[CH:38]=4)[C:35]=3[CH3:36])=[C:28]([S:50]([OH:53])(=O)=[O:51])[CH:27]=[N:26]2)=[CH:21][CH:20]=1)#[N:18].P(Cl)(Cl)(Cl)=O.O.N>C(#N)C.C(OCC)(=O)C.O.N1C=CC=CC=1>[C:17]([C:19]1[CH:24]=[CH:23][C:22]([N:25]2[C:29]([C:30]3[C:31](=[O:49])[N:32]([CH3:48])[C:33](=[O:47])[N:34]([C:37]4[CH:42]=[CH:41][CH:40]=[C:39]([C:43]([F:46])([F:45])[F:44])[CH:38]=4)[C:35]=3[CH3:36])=[C:28]([S:50]([NH2:8])(=[O:53])=[O:51])[CH:27]=[N:26]2)=[CH:21][CH:20]=1)#[N:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 24813Phosphorus oxychlorideHCID 853687(+)-cis-2-BenzylaminocyclohexanemethanolHCID 12896473Azane;hydrateHCID 715138621-(4-cyanophenyl)-5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl)-1H-pyrazole-4-sulfonic acid

生成物 1

HCID 712514151-(4-cyanophenyl)-5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl)-1H-pyrazole-4-sulfonamide

試薬・触媒・溶媒 4

HCID 962Water溶媒HCID 1049Pyridine溶媒HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a suspension of (−)-cis-2-benzylaminocyclohexanemethanol salt of 1-(4-cyanophenyl)-5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl)-1H-pyrazole-4-sulfonic acid (prepared in Example 195) (6.83 g) in acetonitrile (48 ml) were added pyridine (1.47 ml) and phosphorus oxychloride (3.39 ml) and the resulting mixture was stirred at room temperature for two hours. The reaction solution was added dropwise to ammonia water (28%, 48 ml) that cooled to 0° C. and the mixture was stirred for another ten minutes. To the reaction solution were added water (50 ml) and ethyl acetate (100 ml×2) such that the intended products were extracted into an organic layer. The organic layer was washed with 4% ammonia water (50 ml), saturated saline (20 ml), 1N hydrochloric acid (50 ml×2) and saturated saline (50 ml), dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to afford the same product as Example 209, (+)-1-(4-cyanophenyl)-5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl)-1H-pyrazole-4-sulfonamide (4.84 g). UPLC/MS 531 (M+H)/0.87 min. (measurement condition 9)

後処理

  1. temperaturecooled to 0° C.
  2. stirringthe mixture was stirred for another ten minutes
  3. extractionwere extracted into an organic layer
  4. washThe organic layer was washed with 4% ammonia water (50 ml), saturated saline (20 ml), 1N hydrochloric acid (50 ml×2) and saturated saline (50 ml)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-1f596e44ac334c9cb5a4ce090608e140
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09040516B2

反応ノート

読み込み中…

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