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Hydrochloric Acid → (3-chloro-4-{(E)-2-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]vinyl}bicyclo[4.2.1]non-3-en-9-yl)amine

HRID 271307
ノート
印刷プレビュー

反応式

HRID 271307 の反応式
Cl.[Cl:2][C:3]1[CH2:4][CH:5]2[CH:26]([NH:27]S(C(C)(C)C)=O)[CH:8]([CH2:9][C:10]=1/[CH:11]=[CH:12]/[C:13]1[CH:17]=[C:16]([C:18]3[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=3)[N:15]([CH3:25])[N:14]=1)[CH2:7][CH2:6]2>CO>[Cl:2][C:3]1[CH2:4][CH:5]2[CH:26]([NH2:27])[CH:8]([CH2:9][C:10]=1/[CH:11]=[CH:12]/[C:13]1[CH:17]=[C:16]([C:18]3[CH:19]=[CH:20][C:21]([F:24])=[CH:22][CH:23]=3)[N:15]([CH3:25])[N:14]=1)[CH2:7][CH2:6]2
参加物反応条件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 313Hydrochloric AcidHCID 69308312N(3-chloro-4-{(E)2-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]vinyl}bicyclo[4.2.1]non-3-en-9-yl)-2-methylpropane-2-sulfinamide

生成物 1

HCID 69306506(3-chloro-4-{(E)-2-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]vinyl}bicyclo[4.2.1]non-3-en-9-yl)amine収率 84.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
0 °C

実験手順

Hydrochloric acid (in dioxane, 4M, 50 ml) was added into a solution of the product of Step 5 (5.71 g, 12 mmol) in methanol (100 ml) at 0° C. The solution was stirred at 0° C. for 1 hr and then at ambient temperature for a further 1 hr. The reaction mixture was concentrated in vacuo, diluted with saturated sodium hydrogen carbonate and extracted with ethyl acetate (3×100 ml). The organic extract were washed with brine, dried over MgSO4 and concentrated in vacuo, then eluted through an SCX cartridge (50 g) with methanol (100 ml) and then with ammonia in methanol (2M, 50 ml). The fraction containing the product was concentrated in vacuo, to afford (3-chloro-4-{(E)-2-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]vinyl}bicyclo[4.2.1]non-3-en-9-yl)amine (3.76 g, 84%). δH (400 MHz, CDCl3) 1.33-1.61 (4H, m), 1.74-1.92 (2H, m), 2.15-2.23 (1H, br), 2.30-2.39 (1H, br), 2.54-2.69 (3H, m), 3.12 (1H, d, J 18.0), 3.34 (1H, t, J 6.5), 3.82 (3H, s), 6.47 (1H, s), 6.65 (1H, d, J 16.5), 7.15 (2H, t, J 8.5), 7.37-7.41 (2H, m), 7.47 (1H, d, J 16.5)

後処理

  1. waitat ambient temperature for a further 1 hr
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. additiondiluted with saturated sodium hydrogen carbonate
  4. extractionextracted with ethyl acetate (3×100 ml)
  5. extractionThe organic extract
  6. washwere washed with brine
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated in vacuo
  9. washeluted through an SCX cartridge (50 g) with methanol (100 ml)
  10. additionThe fraction containing the product
  11. concentrationwas concentrated in vacuo

出典と根拠

ORDレコード
ord-b927d7787b0a4f17b6e6a888a472b718
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07452899B2

反応ノート

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