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Water → HCID 69410937、化合物

HRID 889847
ノート
印刷プレビュー

反応式

HRID 889847 の反応式
C([O:3][C:4](=[O:35])[CH2:5][N:6]([C:14](=[O:34])[C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([C:21](=[O:33])[NH:22][CH2:23][C:24]2[CH:32]=[CH:31][C:27]3[O:28][CH2:29][O:30][C:26]=3[CH:25]=2)[CH:16]=1)[CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)C.O.O1CCOCC1.[OH-].[Na+]>C(O)C>[O:28]1[C:27]2[CH:31]=[CH:32][C:24]([CH2:23][NH:22][C:21]([C:17]3[CH:16]=[C:15]([CH:20]=[CH:19][CH:18]=3)[C:14]([N:6]([CH2:5][C:4]([OH:35])=[O:3])[CH2:7][C:8]3[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=3)=[O:34])=[O:33])=[CH:25][C:26]=2[O:30][CH2:29]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 312751,4-DioxaneHCID 69411675HCID 69411675、化合物

生成物 1

HCID 69410937HCID 69410937、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
50 °C

実験手順

To a solution of N-benzo[1,3]dioxol-5-ylmethyl-isophthalamic acid (3.0 g, 10 mmol) in methylene chloride was added 1-hydroxy-benzotriazole monohydrate (“HOBt”) (1.35 g, 10 mmol) and ethyl N-benzylglycine (1.94 g, 10 mmol). To this was added 1-(3-dimethylamino-propyl)-3-ethylcarbodiimide hydrochloride (“EDAC”) (1.92 g, 10 mmol) and the mix stirred at room temperature for 24 hours. The solution treated with water (150 mL) and the organic phase separated, washed with 10% citric acid (100 mL), saturated sodium bicarbonate (100 mL) and brine (100 mL). The organic phase dried over magnesium sulfate and evaporated at reduced pressure to give ({3-[(1,3-benzodioxol-5-ylmethyl)-carbamoyl]-benzoyl}-benzyl-amino)-acetic acid ethyl ester as a solid, 3.69 g. To a solution of this ester (3.6 g, 7.6 mmol) in a mix of water (15 mL), dioxane (60 mL) and ethanol (20 mL) was added sodium hydroxide (0.72 g, 18 mmol). The mixture stirred at 50° C. for 24 hours. The solution cooled to room temperature and evaporated at reduced pressure free of solvents. The residue was diluted with water (100 mL) and washed with ether (2×50 mL). The ether discarded and the aqueous phase made acidic with 6N HCl. This was extracted with ethyl acetate (2×100 mL). The organic phases washed with brine (100 mL) and dried over magnesium sulfate. The solvent was evaporated at reduced pressure to give the title compound, 3.41 g. Microanalysis (C25H22N2O6.0.3 H2O): Calc'd: C=66.45, H=5.05, N=6.20. Found: C=66.25, H=5.15, N=5.99.

後処理

  1. temperatureThe solution cooled to room temperature
  2. customevaporated at reduced pressure free of solvents
  3. additionThe residue was diluted with water (100 mL)
  4. washwashed with ether (2×50 mL)
  5. extractionThis was extracted with ethyl acetate (2×100 mL)
  6. washThe organic phases washed with brine (100 mL)
  7. dry with materialdried over magnesium sulfate
  8. customThe solvent was evaporated at reduced pressure

出典と根拠

ORDレコード
ord-d1c267188fdd472c9f190ff540b2a1d5
出典データセット
uspto-grants-2006_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06995151B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート