Hydrochloric Acid → N-(1-(5-amino-2-benzyloxyphenyl)-1-methylethyl)carbamic acid t-butyl ester

HRID 1861971ノート

反応式

HRID 1861971 の反応式
[C:1]([O:5][C:6](=[O:28])[NH:7][C:8]([C:11]1[CH:16]=[C:15]([N+:17]([O-])=O)[CH:14]=[CH:13][C:12]=1[O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)([CH3:10])[CH3:9])([CH3:4])([CH3:3])[CH3:2].[BH4-].[Na+].Cl.C(=O)(O)[O-].[Na+]>O.O.O.O.O.O.[Ni](Cl)Cl.C(Cl)(Cl)Cl.CO>[C:1]([O:5][C:6](=[O:28])[NH:7][C:8]([C:11]1[CH:16]=[C:15]([NH2:17])[CH:14]=[CH:13][C:12]=1[O:20][CH2:21][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)([CH3:10])[CH3:9])([CH3:2])([CH3:3])[CH3:4]

参加物

8

実験手順

To a mixture of the compound (100 mg) obtained in Example 565, nickel (II) chloride hexahydrate (123 mg) and methanol (6 ml), sodium borohydride (39 mg) was added. The reaction mixture was stirred at room temperature for 10 min; then, 2 N HCl was added and a saturated aqueous sodium bicarbonate solution and chloroform were also added. The organic layer was washed with a saturated aqueous sodium chloride solution, dried with anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=3:2) to give 87 mg of the titled compound (yield, 94%).

後処理

  1. additionwas added
  2. washThe organic layer was washed with a saturated aqueous sodium chloride solution
  3. dry with materialdried with anhydrous sodium sulfate
  4. distillationthe solvent was distilled off under reduced pressure
  5. customThe resulting residue was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=3:2)

出典と根拠

ORDレコード
ord-7f84a9a7e5e84b4aa5ba1b129490f017
出典データセット
uspto-grants-2003_03
特許番号
US06534546B1

反応ノート

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