3,4-Dichlorophenyl isocyanate → (3R)-N-(3,4-dichlorophenyl)-4-[(1-ethylpiperidin-3-yl)methyl]-3-methylpiperazine-1-carboxamide

HRID 603187ノート

反応式

HRID 603187 の反応式
[CH3:1][C@H:2]1[NH:7][CH2:6][CH2:5][N:4]([C:8]([O:10]C(C)(C)C)=O)[CH2:3]1.CC1C=CC(S(O[CH2:26][CH:27]2[CH2:32][CH2:31][CH2:30][N:29]([CH2:33][CH3:34])[CH2:28]2)(=O)=O)=CC=1.C(=O)([O-])[O-].[K+].[K+].C(N(C(C)C)CC)(C)C.[Cl:50][C:51]1[CH:52]=[C:53]([N:58]=C=O)[CH:54]=[CH:55][C:56]=1[Cl:57]>C(#N)C.ClCCl>[Cl:50][C:51]1[CH:52]=[C:53]([NH:58][C:8]([N:4]2[CH2:5][CH2:6][N:7]([CH2:26][CH:27]3[CH2:32][CH2:31][CH2:30][N:29]([CH2:33][CH3:34])[CH2:28]3)[C@H:2]([CH3:1])[CH2:3]2)=[O:10])[CH:54]=[CH:55][C:56]=1[Cl:57]

参加物

8

反応物 5

HCID 76073,4-Dichlorophenyl isocyanateHCID 11430Potassium CarbonateHCID 81531DiisopropylethylamineHCID 2756811(R)-1-Boc-3-methylpiperazineHCID 57656762(1-Ethylpiperidin-3-yl)methyl 4-methylbenzenesulfonate

生成物 1

HCID 11531706(3R)-N-(3,4-dichlorophenyl)-4-[(1-ethylpiperidin-3-yl)methyl]-3-methylpiperazine-1-carboxamide収率 67.6%

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 6344Dichloromethane溶媒

反応条件

温度
100 °C

実験手順

To a solution of tert-butyl (3R)-3-methylpiperazine-1-carboxylate (84 mg) and (1-ethylpiperidin-3-yl)methyl 4-methylbenzenesulfonate (150 mg) in acetonitrile (3 mL) was added potassium carbonate (233 mg). The mixture was heated to 100° C. in the microwave for 2 hours and then evaporated. The residue was purified by silica column chromatography, eluting with a gradient of 0 to 5% 7M NH3/MeOH in dichloromethane. To a solution of the isolated material (50 mg) in methanol (5 mL) was added 4M HCl in dioxane (0.5 mL). The mixture was stirred overnight at room temperature and then evaporated to give a colourless oil. To a mixture of this oil in dichloromethane (10 mL) was added di-iso-propylethylamine (0.11 mL) and 3,4-dichlorophenylisocyanate (35 mg). The mixture was stirred for 15 minutes and then evaporated. The residue was purified using reverse phase HPLC eluting with a mixture of 5-95% acetonitrile in water to give the title compound as a white foam (52 mg, 30%).

後処理

  1. customevaporated
  2. customThe residue was purified by silica column chromatography
  3. washeluting with a gradient of 0 to 5% 7M NH3/MeOH in dichloromethane
  4. additionTo a solution of the isolated material (50 mg) in methanol (5 mL) was added 4M HCl in dioxane (0.5 mL)
  5. customevaporated
  6. customto give a colourless oil
  7. stirringThe mixture was stirred for 15 minutes
  8. customevaporated
  9. customThe residue was purified
  10. washeluting with a mixture of 5-95% acetonitrile in water

出典と根拠

ORDレコード
ord-3aab4b2871be433396d4bd480a3dcf79
出典データセット
uspto-grants-2011_03
特許番号
US07906645B2

反応ノート

読み込み中…