Pyrrole-2-Carboxylic Acid → (Pyrrole-2-carbonyl)-N-(benzyl)glycine-t-butyl ester

HRID 362188ノート

反応式

HRID 362188 の反応式
[NH:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([OH:8])=O.C1N(P(Cl)(N2C(=O)OCC2)=O)C(=O)OC1.CCN(C(C)C)C(C)C.[C:33]([O:37][C:38](=[O:48])[CH2:39][NH:40][CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)([CH3:36])([CH3:35])[CH3:34]>ClCCl.C(OCC)(=O)C>[C:33]([O:37][C:38](=[O:48])[CH2:39][N:40]([C:6]([C:2]1[NH:1][CH:5]=[CH:4][CH:3]=1)=[O:8])[CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)([CH3:36])([CH3:34])[CH3:35]

参加物

7

実験手順

To a suspension containing 3.00 g (27.0 mmol) of pyrrole-2-carboxylic acid in 75 mL of anhydrous dichloromethane under a nitrogen atmosphere at 0° C. was added 6.96 g (27.0 mmol of BOPCl and 14.1 mL (81.0 mmol) of DIEA. After stirring for 30 minutes, 5.97 g (27.0 mmol) of N-(benzyl)glycine-t-butyl ester was added and the reaction allowed to warm to room temperature overnight. The reaction was diluted with ethyl acetate and washed with a 5% potassium hydrogensulfate, saturated sodium bicarbonate solution and brine. The organic phase was dried over magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using a gradient of 100% hexane to 60% hexane/ethyl acetate to afford 2.92 g (34.4%) of the title compound is a white solid. FAB MS [M+H] m/z Calcd: 315, Found: 315.

後処理

  1. washwashed with a 5% potassium hydrogensulfate, saturated sodium bicarbonate solution and brine
  2. dry with materialThe organic phase was dried over magnesium sulfate
  3. filtrationfiltered
  4. customevaporated under reduced pressure
  5. customThe residue was purified by column chromatography on silica gel using a gradient of 100% hexane to 60% hexane/ethyl acetate

出典と根拠

ORDレコード
ord-1820661c54d14ba98f6fd55107381985
出典データセット
uspto-grants-1999_02
特許番号
US05869455

反応ノート

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