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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(S)-[1-[[[[4-[[[4,5-Bis(phenylmethoxy)-2-pyridinyl]carbonyl]amino]-2,3-dioxo-1-piperazinyl]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, phenylmethyl ester → (S)-N-[4-[[[(3-Amino-2-oxo-1-azetidinyl)carbonyl]amino]sulfonyl]-2,3-dioxo-1-piperazinyl]-1,4-dihydro-5-hydroxy-4-oxo-2-pyridinecarboxamide

HRID 1252623
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HRID 1252623 반응식
C1(C[O:8][C:9]2[C:14]([O:15]CC3C=CC=CC=3)=[CH:13][N:12]=[C:11]([C:23]([NH:25][N:26]3[CH2:31][CH2:30][N:29]([S:32]([NH:35][C:36]([N:38]4[CH2:41][C@H:40]([NH:42]C(=O)OCC5C=CC=CC=5)[C:39]4=[O:53])=[O:37])(=[O:34])=[O:33])[C:28](=[O:54])[C:27]3=[O:55])=[O:24])[CH:10]=2)C=CC=CC=1>CN(C)C=O.[Pd]>[NH2:42][C@H:40]1[CH2:41][N:38]([C:36]([NH:35][S:32]([N:29]2[CH2:30][CH2:31][N:26]([NH:25][C:23]([C:11]3[NH:12][CH:13]=[C:14]([OH:15])[C:9](=[O:8])[CH:10]=3)=[O:24])[C:27](=[O:55])[C:28]2=[O:54])(=[O:33])=[O:34])=[O:37])[C:39]1=[O:53]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86742167(S)-[1-[[[[4-[[[4,5-Bis(phenylmethoxy)-2-pyridinyl]carbonyl]amino]-2,3-dioxo-1-piperazinyl]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, phenylmethyl ester

생성물 1

HCID 54265560(S)-N-[4-[[[(3-Amino-2-oxo-1-azetidinyl)carbonyl]amino]sulfonyl]-2,3-dioxo-1-piperazinyl]-1,4-dihydro-5-hydroxy-4-oxo-2-pyridinecarboxamide

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 6228Dimethylformamide
용매

실험 절차

To a solution of (S)-[1-[[[[4-[[[4,5-bis(phenylmethoxy)-2-pyridinyl]carbonyl]amino]-2,3-dioxo-1-piperazinyl]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, phenylmethyl ester (1.54 g, 2 mmol) in 30 ml of dimethylformamide was added 0.77 g of palladium on charcoal, and the mixture was hydrogenolyzed for 45 minutes. The catalyst was removed by filtration over Hyflo and the resulting solution was used for the next step without isolation of the title compound.

후처리

  1. customThe catalyst was removed by filtration over Hyflo

출처 및 근거

ORD 기록
ord-d39fbfaef0494495bb4860c36372df88
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04743685

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