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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Morpholino(4-nitro-3-(trifluoromethyl)phenyl)methanone → (4-Amino-3-(trifluoromethyl)phenyl)(morpholino)methanone

HRID 576261
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인쇄 미리보기

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HRID 576261 반응식
[O:1]1[CH2:6][CH2:5][N:4]([C:7]([C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[C:11]([C:18]([F:21])([F:20])[F:19])[CH:10]=2)=[O:8])[CH2:3][CH2:2]1>C(O)C.[Pd]>[NH2:15][C:12]1[CH:13]=[CH:14][C:9]([C:7]([N:4]2[CH2:3][CH2:2][O:1][CH2:6][CH2:5]2)=[O:8])=[CH:10][C:11]=1[C:18]([F:21])([F:20])[F:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68936908Morpholino(4-nitro-3-(trifluoromethyl)phenyl)methanone

생성물 1

HCID 62155530(4-Amino-3-(trifluoromethyl)phenyl)(morpholino)methanone

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of EXAMPLE 144A (13 g) and Pd/C (1.3 g, 10%) in ethanol (300 mL) was stirred under hydrogen at room temperature for two days. The catalyst was filtered off and the solvent was evaporated to provide the final compound.

후처리

  1. filtrationThe catalyst was filtered off
  2. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-a1fedb24226f4d35b15c710dba55d528
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09035047B2

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