Methanol → 4-{[2-(Benzyloxy)-2-oxoethyl]amino}-adamantane-1-carboxylic acid

HRID 1515350노트

반응식

HRID 1515350 반응식
[CH2:1]([O:8][C:9](=[O:26])[CH2:10][NH:11][CH:12]1[CH:19]2[CH2:20][C:15]3([C:22]([O:24]C)=[O:23])[CH2:16][CH:17]([CH2:21][CH:13]1[CH2:14]3)[CH2:18]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CO.[OH-].[Na+]>O1CCCC1>[CH2:1]([O:8][C:9](=[O:26])[CH2:10][NH:11][CH:12]1[CH:19]2[CH2:20][C:15]3([C:22]([OH:24])=[O:23])[CH2:16][CH:17]([CH2:21][CH:13]1[CH2:14]3)[CH2:18]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

5

실험 절차

To a suspension of methyl 4-{[2-(benzyloxy)-2-oxoethyl]amino}-adamantane-1-carboxylate thus obtained (3.30 g) in tetrahydrofuran (20 ml), methanol (10 ml) and 8M aqueous sodium hydroxide (10 ml) were added and stirred at room temperature for 3 hours. After the reaction mixture was concentrated, the resulting residue was diluted with 1M aqueous sodium hydroxide and washed with diethyl ether. The resulting aqueous layer was diluted with 12M aqueous hydrochloric acid and extracted with chloroform. The organic layer was washed with brine and then dried over anhydrous sodium sulfate. After the desiccant was filtered off, the solvent was distilled off under reduced pressure to give 4-{[2-(benzyloxy)-2-oxoethyl]amino}-adamantane-1-carboxylic acid (2.95 g) as a light-brown viscous substance.

후처리

  1. concentrationAfter the reaction mixture was concentrated
  2. additionthe resulting residue was diluted with 1M aqueous sodium hydroxide
  3. washwashed with diethyl ether
  4. additionThe resulting aqueous layer was diluted with 12M aqueous hydrochloric acid
  5. extractionextracted with chloroform
  6. washThe organic layer was washed with brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationAfter the desiccant was filtered off
  9. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-ebf1f60804e549be95aae619d1e3e15f
출처 데이터셋
uspto-grants-2012_07
특허 번호
US08222417B2

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