Hydrochloric Acid → N-(9-ethyl-9H-carbazol-3-yl)-3,5-dihydroxy-3-methylpentanamide

HRID 2272592

反応式

HRID 2272592 の反応式
[CH2:1]([N:3]1[C:15]2[CH:14]=[CH:13][C:12]([NH2:16])=[CH:11][C:10]=2[C:9]2[C:4]1=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH3:2].C[Al](C)C.[OH:21][C:22]1([CH3:29])[CH2:27][CH2:26][O:25][C:24](=[O:28])[CH2:23]1.Cl>C1(C)C=CC=CC=1>[CH2:1]([N:3]1[C:15]2[CH:14]=[CH:13][C:12]([NH:16][C:24](=[O:28])[CH2:23][C:22]([OH:21])([CH3:29])[CH2:27][CH2:26][OH:25])=[CH:11][C:10]=2[C:9]2[C:4]1=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH3:2]

参加物

6

実験手順

To a solution of 9-ethyl-9H-carbazol-3-amine (300 mg, 1.43 mmol) in toluene (4 mL) was added trimethylaluminium (1.8M in toluene solution, 1.189 mL, 2.14 mmol), and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added a solution of 4-hydroxy-4-methyltetrahydro-2H-pyran-2-one (186 mg, 1.43 mmol) in toluene (4 mL) at room temperature, and the mixture was stirred at 80° C. for 4 hr. The reaction mixture was cooled to 0° C., neutralized with 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 10 to 100% ethyl acetate/hexane) to give N-(9-ethyl-9H-carbazol-3-yl)-3,5-dihydroxy-3-methylpentanamide (359 mg, 1.056 mmol, 74.0%) as a colorless oil.

後処理

  1. stirringthe mixture was stirred at 80° C. for 4 hr
  2. temperatureThe reaction mixture was cooled to 0° C.
  3. extractionextracted with ethyl acetate
  4. washThe organic layer was washed with water and saturated brine
  5. customdried
  6. customthe solvent was evaporated under reduced pressure
  7. customThe obtained residue was purified by silica gel column chromatography (solvent gradient; 10 to 100% ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-c4387e4ab56f497e9361dcd751b5d166
出典データセット
uspto-grants-2015_09
特許番号
US09120776B2

関連ノート

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