ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

P-Toluenesulfonamide → methyl (2E)-3-(4-bromophenyl)-2-({[(4-methylphenyl)sulfonyl]amino}methyl)-2-propenoate

HRID 2423393
ノート
印刷プレビュー

反応式

HRID 2423393 の反応式
C(Cl)(=O)C.[Br:5][C:6]1[CH:11]=[CH:10][C:9]([CH:12](O)[C:13](=[CH2:18])[C:14]([O:16][CH3:17])=[O:15])=[CH:8][CH:7]=1.[CH3:20][C:21]1[CH:26]=[CH:25][C:24]([S:27]([NH2:30])(=[O:29])=[O:28])=[CH:23][CH:22]=1.C([O-])([O-])=O.[K+].[K+]>C1COCC1.CCOC(C)=O>[Br:5][C:6]1[CH:11]=[CH:10][C:9](/[CH:12]=[C:13](\[CH2:18][NH:30][S:27]([C:24]2[CH:25]=[CH:26][C:21]([CH3:20])=[CH:22][CH:23]=2)(=[O:28])=[O:29])/[C:14]([O:16][CH3:17])=[O:15])=[CH:8][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6269P-ToluenesulfonamideHCID 6367Acetyl chloride2 回HCID 11430Potassium CarbonateHCID 603917Methyl 2-((4-bromophenyl)(hydroxy)methyl)acrylate

生成物 1

HCID 59321496methyl (2E)-3-(4-bromophenyl)-2-({[(4-methylphenyl)sulfonyl]amino}methyl)-2-propenoate収率 37.2%

試薬・触媒・溶媒 2

HCID 8028
Tetrahydrofuran
溶媒
2 回
HCID 8857Ethyl Acetate溶媒2 回

実験手順

To a solution of 390 μL (5.46 mmol) of acetyl chloride in 10 mL of THF at 0° C. was added 1.41 g (5.20 mmol) of methyl 2-[(4-bromophenyl)(hydroxy)methyl]-2-propenoate and 870 μL (6.24 mmol) of TEA in 10 mL THF. After 2 hr at ambient temperature another 870 μL (6.24 mmol) of TEA and 390 μL (5.46 mmol) of acetyl chloride was added and the solution stirred at ambient temperature for an additional 1 hr. EtOAc was added and the organics washed with three 50 mL portions of H2O then 50 mL of brine. The organics were dried over Na2SO4 then concentrated. This residue was then taken up in 25 mL of DMF and 4.35 g (25.4 mmol) of 4-methylbenzenesulfonamide and 3.51 g (25.4 mmol) of K2CO3 were added. The mixture was stirred at 50° C. for 3 hr. To the mixture was added 100 mL of EtOAc which was then washed with three 50 mL portions of water, then brine. The solution was concentrated and the residue purified by silica gel chromatography (120 g of silica gel eluting with 0-40% EtOAc in hexanes over 45 minutes) to give 820 mg (37%) of methyl (2E)-3-(4-bromophenyl)-2-({[(4-methylphenyl)sulfonyl]amino}methyl)-2-propenoate as a beige glass. 1H NMR (400 MHz, CDCl3): δ 7.68-7.66 (m, 3H), 7.52 (d, J=7 Hz, 2H), 7.29-7.25 (m, 4H), 5.51 (t, J =6 Hz, 1H), 3.86 (d, J=6 Hz, 2H), 3.75 (s, 3H), 2.43 (s, 3H). ESI-LCMS m/z 425 (M+H)+.

後処理

  1. washthe organics washed with three 50 mL portions of H2O
  2. dry with materialThe organics were dried over Na2SO4
  3. concentrationthen concentrated
  4. stirringThe mixture was stirred at 50° C. for 3 hr
  5. washwas then washed with three 50 mL portions of water
  6. concentrationThe solution was concentrated
  7. customthe residue purified by silica gel chromatography (120 g of silica gel eluting with 0-40% EtOAc in hexanes over 45 minutes)

出典と根拠

ORDレコード
ord-47da0c31013e4b0c8b182fb3d437bfc8
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07960552B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート