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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-(4-Nitrobenzyl)imidazolidine-2,4-dione → 3-[(4-Aminophenyl)methyl]imidazolidine-2,4-dione

HRID 2270106
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인쇄 미리보기

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HRID 2270106 반응식
[N+:1]([C:4]1[CH:17]=[CH:16][C:7]([CH2:8][N:9]2[C:13](=[O:14])[CH2:12][NH:11][C:10]2=[O:15])=[CH:6][CH:5]=1)([O-])=O>CO.[Pd].[H][H]>[NH2:1][C:4]1[CH:17]=[CH:16][C:7]([CH2:8][N:9]2[C:13](=[O:14])[CH2:12][NH:11][C:10]2=[O:15])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 107522073-(4-Nitrobenzyl)imidazolidine-2,4-dione

생성물 1

HCID 106558433-[(4-Aminophenyl)methyl]imidazolidine-2,4-dione

시약·촉매·용매 3

HCID 887Methanol용매HCID 23938Palladium용매HCID 178418361HCID 178418361, 화합물용매

실험 절차

The 3-(4-nitrobenzyl)hydantoin derivative as dissolved in methanol (about 10 ml per mmol of hydantoin derivative) and hydrogenated with palladium/carbon in a hydrogen atmosphere until reaction was complete. The catalyst was filtered off and the solvent was removed on a rotary evaporator. The 3-(4-aminobenzyl)hydantoin derivative was obtained.

후처리

  1. filtrationThe catalyst was filtered off
  2. customthe solvent was removed on a rotary evaporator

출처 및 근거

ORD 기록
ord-c31f846a3aad43c1a475eae085db9853
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06331552B1

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