Dicyclohexylcarbodiimide → HCID 21463059, 화합물

HRID 374999

반응식

HRID 374999 반응식
[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]

참가 물질

7

실험 절차

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 filtrate 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).

후처리

  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 filtrate 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

출처 및 근거

ORD 기록
ord-0ae52ed9dc254deaa9ffde3f0b954e69
출처 데이터셋
uspto-grants-1996_01
특허 번호
US05482967

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