1-((tert-Butoxycarbonyl)amino)cyclopropanecarboxylic acid → 2,5-Dimethylcyclopentyl N-t-butoxycarbonyl-1-aminocyclopropanecarboxylate

HRID 35444

反応式

HRID 35444 の反応式
[CH3:1][CH:2]1[CH2:6][CH2:5][CH:4]([CH3:7])[CH:3]1[OH:8].[C:9]([O:13][C:14]([NH:16][C:17]1([C:20](O)=[O:21])[CH2:19][CH2:18]1)=[O:15])([CH3:12])([CH3:11])[CH3:10]>CN(C)C1C=CN=CC=1.C(Cl)Cl>[C:9]([O:13][C:14]([NH:16][C:17]1([C:20]([O:8][CH:3]2[CH:4]([CH3:7])[CH2:5][CH2:6][CH:2]2[CH3:1])=[O:21])[CH2:19][CH2:18]1)=[O:15])([CH3:12])([CH3:11])[CH3:10]

参加物

5

実験手順

To a solution of 2,5-dimethylcyclopentanol (0.55 g.), compound 1 (0.97 g), and 4-(dimethylamino)pyridine (0.06 g.) in methylene chloride (100 ml) was added dicyclohexylacarbodiimide (1.09 g.), and the resulting mixture was stirred overnight. The precipitated dicyclohexylurea was removed by filtration, and the filtrate was evaporated. Ethyl acetate was then added to the residue, and the mixture was filtered again. The filtrate was washed with 1M hydrochloric acid, saturated aqeuous sodium bicarbonate, and water, dried over magnesium sulfate, and the solvent was evaporated to a colorless oil (1.18 g. 83%). The product was purified by column chromotography on silica gel, 4:1 hexane:ethyl acetate, eluent.

後処理

  1. customThe precipitated dicyclohexylurea was removed by filtration
  2. customthe filtrate was evaporated
  3. additionEthyl acetate was then added to the residue
  4. filtrationthe mixture was filtered again
  5. washThe filtrate was washed with 1M hydrochloric acid, saturated aqeuous sodium bicarbonate, and water
  6. dry with materialdried over magnesium sulfate
  7. customthe solvent was evaporated to a colorless oil (1.18 g. 83%)
  8. customThe product was purified by column chromotography on silica gel, 4:1 hexane

出典と根拠

ORDレコード
ord-c25432ba33814242995d179d36701e13
出典データセット
uspto-grants-1988_08
特許番号
US04766246

関連ノート

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