Phosphorus oxychloride → HCID 19921455, 화합물

HRID 1647897노트

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HRID 1647897 반응식
[CH3:1][O:2][C:3]([CH2:5][CH2:6][NH:7][C:8](=[O:18])[C:9]1[CH:14]=[CH:13][C:12]([NH:15][CH3:16])=[C:11]([NH2:17])[CH:10]=1)=[O:4].P(Cl)(Cl)(Cl)=O.[C:24]([C:26]1[CH:34]=[CH:33][C:29]([C:30](Cl)=O)=[CH:28][CH:27]=1)#[N:25]>C(OCC)(=O)C>[C:24]([C:26]1[CH:34]=[CH:33][C:29]([C:30]2[N:15]([CH3:16])[C:12]3[CH:13]=[CH:14][C:9]([C:8]([NH:7][CH2:6][CH2:5][C:3]([O:2][CH3:1])=[O:4])=[O:18])=[CH:10][C:11]=3[N:17]=2)=[CH:28][CH:27]=1)#[N:25]

참가 물질

5

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온도
90 °C

실험 절차

4.7 g of 3-amino-4-methylamino-benzoic acid-[N-(2-methoxycarbonyl-ethyl)-amide] are first stirred at ambient temperature with 40 ml of phosphorusoxychloride, then 3.1 g of 4-cyano-benzoylchloride are added and the mixture is heated to 90° C. for 8 hours. The phosphorusoxychloride is distilled off in vacuo, the residue is stirred into 500 ml of water at 30° C. and neutralised by the addition of sodium bicarbonate in batches. The precipitate is suction filtered and extracted with ethyl acetate. The ethyl acetate phases are evaporated down, the residue is combined with the precipitate and purified by chromatography on silica gel (eluant:ethyl acetate/ethanol=100:1 to 100:5). The product obtained is decocted with ethyl acetate for final purification. Yield: 1,86 g (27% of theory), Rf value: 0.51 (silica gel; ethyl acetate/ethanol=9:1)

후처리

  1. distillationThe phosphorusoxychloride is distilled off in vacuo
  2. additionneutralised by the addition of sodium bicarbonate in batches
  3. filtrationfiltered
  4. extractionextracted with ethyl acetate
  5. customThe ethyl acetate phases are evaporated down
  6. custompurified by chromatography on silica gel (eluant:ethyl acetate/ethanol=100:1 to 100:5)
  7. customThe product obtained
  8. custompurification

출처 및 근거

ORD 기록
ord-8b67c3c662884c7497ee85ea4ab992cf
출처 데이터셋
uspto-grants-1995_07
특허 번호
US05434150

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