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Diethyl Ether → HCID 131713874, 화합물

HRID 1632420
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HRID 1632420 반응식
[NH:1]([C:23]([O:25][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)=[O:24])[C@H:2]([C:5]([NH:7][C@H:8]([C:13]([NH:15][C@H:16]([C:19](OC)=[O:20])[CH2:17][OH:18])=[O:14])[CH2:9][CH:10]([CH3:12])[CH3:11])=[O:6])[CH2:3]O.[NH2:33][NH2:34].[OH2:35].CCOCC>CO>[NH:1]([C:23]([O:25][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)=[O:24])[C@H:2]([C:5]([NH:7][C@H:8]([C:13]([NH:15][C@H:16]([C:17]([NH:33][NH2:34])=[O:18])[CH2:19][OH:20])=[O:14])[CH2:9][CH:10]([CH3:12])[CH3:11])=[O:6])[CH2:3][OH:35]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 24654Hydrazine hydrate (1:1)HCID 91978513Z-Ser-Leu-Ser-OCH3

생성물 1

HCID 131713874HCID 131713874, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

2.00 Grams of Z-Ser-Leu-Ser-OCH3 was dissolved in 40 ml of methanol, then 1.10 ml of 100%-NH2NH2.H2O was added to the solution under ice-cooled condition, and the reaction mixture was allowed to stand at a room temperature for 18 hours. After completion of the reaction, the solvent was removed by distillation under a reduced pressure, and the residue obtained was solidified by adding ether, then an excess of NH2NH2.H2O was removed by adding water, then reprecipitated from methanol-ethyl acetate to obtain 1.91 g of the desired product.

후처리

  1. temperaturecooled condition
  2. customAfter completion of the reaction
  3. customthe solvent was removed by distillation under a reduced pressure
  4. customthe residue obtained
  5. customan excess of NH2NH2.H2O was removed
  6. additionby adding water
  7. customreprecipitated from methanol-ethyl acetate

출처 및 근거

ORD 기록
ord-d8d48c719aff4241a992fd40c0d9efb8
출처 데이터셋
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04474754

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