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N-Benzyloxycarbonyl-phenylalanine glycine-methylester → Cyclo(-Gly-Phe)

HRID 25853
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인쇄 미리보기

반응식

HRID 25853 반응식
C([O:8][C:9]([NH:11][C@H:12]([C:20]([OH:22])=O)[CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=O)C1C=CC=CC=1.COC(=O)[CH2:26][NH2:27]>CO.[Pd]>[CH2:13]([C@@H:12]1[NH:11][C:9](=[O:8])[CH2:26][NH:27][C:20]1=[O:22])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 69129857N-Benzyloxycarbonyl-phenylalanine glycine-methylester

생성물 1

HCID 7076549Cyclo(-Gly-Phe)수율 83.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A solution of 23.30 g (62.91 mmol) N-Benzyloxycarbonyl-phenylalanine-glycine-methylester (obtained above) in 650 ml dry methanol was hydrogenated by adding Pd/C-catalyst and stirring the resulting mixture under H2 at r.t. for 3 h. After that, the mixture was filtered through celite and then half of the solvent was evaporated. The remaining solution was refluxed for 17 h. Filtration of the white precipitate and washing it twice with methanol yielded 10.71 g (52.45 mmol, 83.37%) 6-(S)-Benzyl-piperazine-2,5-dione as a white solid.

후처리

  1. filtrationAfter that, the mixture was filtered through celite
  2. customhalf of the solvent was evaporated
  3. temperatureThe remaining solution was refluxed for 17 h
  4. filtrationFiltration of the white precipitate
  5. washwashing it twice with methanol

출처 및 근거

ORD 기록
ord-bc3c826f7798473c9968d89d218e17b6
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06858600B2

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