Water → 2-Methyloctanamide

HRID 1358692ノート

反応式

HRID 1358692 の反応式
CO[C:3]1[CH:13]=[CH:12][C:6]([CH2:7]SCCN)=[CH:5][CH:4]=1.[CH2:14]([N:16](CC)CC)C.[OH2:21].Cl[CH2:23]Cl>>[CH3:23][CH:7]([C:14]([NH2:16])=[O:21])[CH2:6][CH2:12][CH2:13][CH2:3][CH2:4][CH3:5]

参加物

5

反応条件

温度
-10 °C

実験手順

The [1RS-(2-exo,3-exo)]-3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octane-2-carbonyl chloride 21 obtained in Example 17 was dissolved in 10 ml of dichloromethane, and the solution was cooled to −10° C. A solution of 197 mg (1 mmol) of 4-methoxybenzylthioethylamine in 10 ml of dichloromethane and then 0.28 ml (2 mmol) of triethylamine were added thereto under nitrogen, and the resulting mixture was stirred at room temperature for 6 hours. Thereafter, 20 ml of water was added thereto and the desired compound was extracted three times with dichloromethane. The combined organic layer was dried over sodium sulfate and then distilled to remove the solvent. The oil thus obtained was purified by silica gel column chromatography (eluent: ethyl acetate/methanol/aqueous ammonia=8.5/1/0.5) to obtain [1RS-(2-exo,3-exo)]-3-(4-chlorophenyl)-N-[2-[S-(4-methoxybenzyl)thio]ethyl]-8-methyl-8-azabicyclo[3.2.])-octane-2-carboxamide as an oil.

後処理

  1. extractionthe desired compound was extracted three times with dichloromethane
  2. dry with materialThe combined organic layer was dried over sodium sulfate
  3. distillationdistilled
  4. customto remove the solvent
  5. customThe oil thus obtained
  6. customwas purified by silica gel column chromatography (eluent: ethyl acetate/methanol/aqueous ammonia=8.5/1/0.5)

出典と根拠

ORDレコード
ord-6c27f3be207a4277b934ebec620c0172
出典データセット
uspto-grants-2003_07
特許番号
US06596868B2

反応ノート

読み込み中…