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3-{4-[(3-Fluorophenyl)methoxy]phenyl}-N-methylbut-2-enamide → HCID 10447594, 화합물

HRID 2184372
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인쇄 미리보기

반응식

HRID 2184372 반응식
[CH3:1][NH:2][C:3](=[O:22])[CH:4]=[C:5]([C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([F:21])[CH:16]=2)=[CH:9][CH:8]=1)[CH3:6]>CO.[Pt]>[F:21][C:17]1[CH:16]=[C:15]([CH:20]=[CH:19][CH:18]=1)[CH2:14][O:13][C:10]1[CH:9]=[CH:8][C:7]([CH:5]([CH3:6])[CH2:4][C:3]([NH:2][CH3:1])=[O:22])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 692909953-{4-[(3-Fluorophenyl)methoxy]phenyl}-N-methylbut-2-enamide

생성물 1

HCID 10447594HCID 10447594, 화합물수율 81.5%

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 887Methanol용매

실험 절차

100 mg (0.33 mmol) of 3-[4-(3-fluoro-benzyloxy)-phenyl]-but-2-enoic acid methylamide is dissolved in 7 ml methanol. 25 mg of platinum 5% on charcoal is added and the mixture is hydrogenated at RT and normal pressure. The catalyst is filtered off and the filtrate evaporated to dryness, leaving 81 mg of a colorless solid. MS: m/e=302.3 (M++H).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customis hydrogenated at RT
  2. filtrationThe catalyst is filtered off
  3. customthe filtrate evaporated to dryness

출처 및 근거

ORD 기록
ord-9fa4fdc808ae405db5b650cd761bd54c
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06900354B2

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