Dicyclohexylcarbodiimide → N-[2-(4-fluorobenzoyl)benzoyl]-N-methylglycine ethyl ester

HRID 1940966ノート

反応式

HRID 1940966 の反応式
[F:1][C:2]1[CH:18]=[CH:17][C:5]([C:6]([C:8]2[CH:16]=[CH:15][CH:14]=[CH:13][C:9]=2[C:10]([OH:12])=O)=[O:7])=[CH:4][CH:3]=1.ON1C2C=CC=CC=2N=N1.C1(N=C=NC2CCCCC2)CCCCC1.Cl.[CH2:45]([O:47][C:48](=[O:52])[CH2:49][NH:50][CH3:51])[CH3:46]>C(N(CC)CC)C.C1COCC1>[CH2:45]([O:47][C:48](=[O:52])[CH2:49][N:50]([C:10](=[O:12])[C:9]1[CH:13]=[CH:14][CH:15]=[CH:16][C:8]=1[C:6](=[O:7])[C:5]1[CH:4]=[CH:3][C:2]([F:1])=[CH:18][CH:17]=1)[CH3:51])[CH3:46]

参加物

7

実験手順

A mixture of 2-(4-fluorobenzoyl)benzoic acid (3.00 g), 1-hydroxybenzotriazole (2.07 g), 1,3-dicyclohexylcarbodiimide (3.00 g) and anhydrous THF (50 ml) was stirred at room temperature for 1 hour. To this mixture were added N-methylglycine ethyl ester hydrochloride (2.84 g) and triethylamine (2.58 ml), followed by stirring at room temperature for 16 hours and with heating and refluxing for 4 hours. After the solvent was distilled off, ethyl acetate was added to the residue, and the insoluble crystals were separated by filtration. The flitrate was washed successively with water, aqueous sodium hydrogen carbonate, water, dilute hydrochloric acid and water and then dried, after which the solvent was distilled off, to yield N-[2-(4-fluorobenzoyl)benzoyl]-N-methylglycine ethyl ester as a colorless oily substance (4.2 g).

後処理

  1. stirringby stirring at room temperature for 16 hours
  2. temperaturewith heating
  3. temperaturerefluxing for 4 hours
  4. distillationAfter the solvent was distilled off
  5. additionethyl acetate was added to the residue
  6. customthe insoluble crystals were separated by filtration
  7. washThe flitrate was washed successively with water, aqueous sodium hydrogen carbonate, water, dilute hydrochloric acid and water
  8. customdried
  9. distillationafter which the solvent was distilled off

出典と根拠

ORDレコード
ord-b116d25aeebc42b588904429ff35c998
出典データセット
uspto-grants-1997_12
特許番号
US05700810

反応ノート

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