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

HRID 271308
ノート
印刷プレビュー

反応式

HRID 271308 の反応式
[Cl:1][C:2]1[CH2:3][CH:4]2[CH:25]([NH2:26])[CH:7]([CH2:8][C:9]=1/[CH:10]=[CH:11]/[C:12]1[CH:16]=[C:15]([C:17]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=3)[N:14]([CH3:24])[N:13]=1)[CH2:6][CH2:5]2.C(N([CH2:32][CH3:33])CC)C.C([NH:37][S:38](Cl)(=[O:40])=[O:39])CC.[CH2:42](Cl)Cl>O>[Cl:1][C:2]1[CH2:3][CH:4]2[CH:25]([N:26]([CH2:42][CH2:32][CH3:33])[S:38]([NH2:37])(=[O:40])=[O:39])[CH:7]([CH2:8][C:9]=1/[CH:10]=[CH:11]/[C:12]1[CH:16]=[C:15]([C:17]3[CH:18]=[CH:19][C:20]([F:23])=[CH:21][CH:22]=3)[N:14]([CH3:24])[N:13]=1)[CH2:6][CH2:5]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 4

HCID 6344DichloromethaneHCID 8471TriethylamineHCID 13398949N-propylsulfamoyl chlorideHCID 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

生成物 1

HCID 69306475N-(3-chloro-4-{(E)-2-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]vinyl}bicyclo[4.2.1]non-3-en-9-yl)-N-propylsulfamide収率 74%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of the product from Step 6 (100 mg, 0.27 mmol), triethylamine (110 mg, 1.1 mmol) and propylsulfamoyl chloride (170 mg, 1.1 mmol) in DCM (5 ml) was stirred at ambient temperature for 18 hrs. The reaction mixture was diluted with water (20 ml) and extracted with ethyl acetate (3×20 ml). The organic extracts were washed with brine (50 ml), dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate: hexane (1:4) to afford N-(3-chloro-4-{(E)-2-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]vinyl}bicyclo[4.2.1]non-3-en-9-yl)-N-propylsulfamide (98 mg, 74%). δH (400 MHz, CDCl3) 0.98 (3H, t, J 7.5), 1.42-1.48 (1H, m), 1.54-1.62 (4H, m), 1.82-1.90 (2H, m), 2.38-2.62 (3H, m), 2.68-2.76 (2H, m), 2.98-3.08 (3H, m), 3.72-3.77 (1H, m), 3.82 (2H, s), 4.13-4.18 (1H, m), 4.33 (1H, d, J 9.0), 6.48 (1H, s), 6.64 (1H, d, J 16.5), 7.12-7.18 (2H, m), 7.37-7.43 (2H, m), 7.45 (1H, d, J 16.5).

後処理

  1. extractionextracted with ethyl acetate (3×20 ml)
  2. washThe organic extracts were washed with brine (50 ml)
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by flash chromatography
  6. washeluting with ethyl acetate: hexane (1:4)

出典と根拠

ORDレコード
ord-6bf65542364b49848b57f2a5c70c450d
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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