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1,4-Dioxane → HCID 131734353、化合物

HRID 1505710
ノート
印刷プレビュー

反応式

HRID 1505710 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([N:14]2[CH:18]=[C:17]([C:19]3[CH:20]=[N:21][C:22]([C:25]4[CH:30]=[CH:29][CH:28]=[C:27]([C:31]#[C:32][Si](C)(C)C)[CH:26]=4)=[N:23][CH:24]=3)[CH:16]=[N:15]2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[N:37]([CH2:40][Si:41]([CH3:44])([CH3:43])[CH3:42])=[N+:38]=[N-:39].[CH2:45]1OCCOC1>O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Cu+2]>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][CH:11]([N:14]2[CH:18]=[C:17]([C:19]3[CH:24]=[N:23][C:22]([C:25]4[CH:30]=[CH:29][CH:28]=[C:27]([C:31]5[N:39]=[N:38][N:37]([CH:40]([Si:41]([CH3:44])([CH3:43])[CH3:42])[CH3:45])[CH:32]=5)[CH:26]=4)=[N:21][CH:20]=3)[CH:16]=[N:15]2)[CH2:12][CH2:13]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 312751,4-DioxaneHCID 150751Trimethylsilylmethyl AzideHCID 89924168HCID 89924168、化合物2 回

生成物 1

HCID 131734353HCID 131734353、化合物収率 49%

試薬・触媒・溶媒 2

HCID 24463Copper sulfate pentahydrate触媒HCID 962
Water
溶媒
2 回

実験手順

A solution of copper sulfate pentahydrate (2.2 mg; 0.01 mmol; 0.04 eq.) in water (0.2 mL) was added to a mixture of 4-{4-[2-(3-Trimethylsilanylethynyl-phenyl)-pyrimidin-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester (intermediate 19, 110 mg; 0.22 mmol; 1.0 eq.), azidomethyl-trimethyl-silane (36 μl; 0.24 mmol; 1.1 eq.) and D-(−)-isoascorbic acid sodium salt (9 mg; 0.04 mmol; 0.2 eq.) in Dioxane-1,4 (3 mL). The vial was sealed and stirred overnight at 8000. The reaction mixture was then diluted with water and extracted with EtOAc (three times). Combined organic phases were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by flash chromatography on silica afforded the title compound as a beige solid (60 mg, 49%). 1H NMR (300 MHz, DMSO-d6) δ 9.18 (s, 2H), 8.88 (t, J=1.6 Hz, 1H), 8.57 (s, 1H), 8.54 (s, 1H), 8.34 (dt, J=8.0 Hz, 1.6 Hz, 1H), 8.16 (s, 1H), 7.96 (dt, J=8.0 Hz, 1.6 Hz, 1H), 7.60 (t, J=8.0 Hz, 1H), 4.48-4.38 (m, 1H), 4.11-4.03 (m, 4H), 2.94 (m, 2H), 2.09-2.05 (m, 2H), 1.88-1.74 (m, 2H), 1.43 (s, 9H), 0.13 (s, 9H). MS (ESI+): 559.5.

後処理

  1. customThe vial was sealed
  2. extractionextracted with EtOAc (three times)
  3. washCombined organic phases were washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customPurification by flash chromatography on silica

出典と根拠

ORDレコード
ord-0d18d58fcf1341818182a633c6855354
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09216991B2

反応ノート

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