Sodium hydride → N-(N-[1-Methoxycarbonylethyl]carbamoyl)-2-phenylethenesulfonamide

HRID 461467

반응식

HRID 461467 반응식
Cl.[CH3:2][O:3][C:4](=[O:8])[CH:5]([CH3:7])[NH2:6].[H-].[Na+].C1(N(C2C=CC=CC=2)[C:18]([NH:20][S:21]([CH:24]=[CH:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)(=[O:23])=[O:22])=[O:19])C=CC=CC=1.C1(C=CS(N)(=O)=O)C=CC=CC=1>CCOCC.CN(C)C=O>[CH3:2][O:3][C:4]([CH:5]([NH:6][C:18]([NH:20][S:21]([CH:24]=[CH:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)(=[O:23])=[O:22])=[O:19])[CH3:7])=[O:8]

참가 물질

7

반응물 4

HCID 24758Sodium hydrideHCID 2575012-PhenylethenesulfonamideHCID 2756298Alanine, methyl ester, hydrochloride (1:1)HCID 53928905N-(Diphenylcarbamoyl)-2-phenylethene-1-sulfonamide

생성물 1

HCID 54315961N-(N-[1-Methoxycarbonylethyl]carbamoyl)-2-phenylethenesulfonamide

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 6228Dimethylformamide용매

실험 절차

To a solution of 3.5 g. of DL-alanine methyl ester hydrochloride in 20 ml. of N,N-dimethylformamide is added 1.05 g. of a 56.6% suspension of sodium hydride in mineral oil. The mixture is stirred at ambient temperature for 15 minutes, and then 3.8 g. of N-(N,N-diphenylcarbamoyl)-2-phenylethenesulfonamide is added. The whole reaction mixture is then maintained at ca. 90° C. for 40 minutes. After being allowed to cool to room temperature, it is diluted with an excess of ether and then it is extracted with water. Acidification of the water extract with dilute hydrochloric acid causes precipitation of the crude product, which is then filtered off. The ether phase is washed with dilute hydrochloric acid, which causes a further crop of product to precipitate. It is filtered off and the two crops of product are combined. This yields 1.55 g. of material having a melting point of 135°-139° C. The crude product is recrystallized from a mixture of acetone and hexane, giving 0.70 g. of N-[N-1-methoxycarbonylethyl)carbamoyl]-2-phenylethenesulfonamide, m.p. 138°-140° C.

후처리

  1. customThe whole reaction mixture
  2. temperatureis then maintained at ca. 90° C. for 40 minutes
  3. temperatureto cool to room temperature
  4. extractionit is extracted with water
  5. extractionAcidification of the water extract with dilute hydrochloric acid
  6. customprecipitation of the crude product, which
  7. filtrationis then filtered off
  8. washThe ether phase is washed with dilute hydrochloric acid, which
  9. customto precipitate
  10. filtrationIt is filtered off
  11. customThe crude product is recrystallized from a mixture of acetone and hexane
  12. customgiving 0.70 g

출처 및 근거

ORD 기록
ord-fbdc6335ce0c4e079f14a8f6a4bd4bd3
출처 데이터셋
uspto-grants-1977_12
특허 번호
US04062960

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