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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 20522463, 화합물 → L-Phenylalanyl-L-valine

HRID 223096
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HRID 223096 반응식
C[O:2][C:3]([CH:5]([N:9]1[CH:12]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:11]([N:19]=[N+]=[N-])[C:10]1=[O:22])[CH:6]([CH3:8])[CH3:7])=[O:4]>C(O)C.[Pd]>[NH2:19][C@H:11]([C:10]([NH:9][C@H:5]([C:3]([OH:4])=[O:2])[CH:6]([CH3:8])[CH3:7])=[O:22])[CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 20522463HCID 20522463, 화합물

생성물 1

HCID 7359122L-Phenylalanyl-L-valine수율 86.5%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

According to the same procedure as in Example 1, 1-(1-methoxycarbonyl-2-methylpropyl)-3-azido-4-phenylazetidin-2-one (500 mg.) was subjected to hydrogenolysis at 50° C. in ethanol (30 ml.) under a hydrogen pressure of one atmosphere in the presence of a 10% Pd-C (175 mg.). The reaction was completed in 19 hours. The same after-treatment as in Example 1 was followed to give methyl ester of phenylalanylvaline (378 mg., yield: 81.9%), which was an oil.

출처 및 근거

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트
ORD 기록
ord-778e8cab8f99449983ec5210f00cdb83
출처 데이터셋
uspto-grants-1982_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04352752

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