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2-Nitro-5-(3-oxo-morpholin-4-yl)-benzonitrile → 2-Amino-5-(3-oxo-morpholin-4-YL)-benzonitrile

HRID 1819530
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인쇄 미리보기

반응식

HRID 1819530 반응식
[N+:1]([C:4]1[CH:11]=[CH:10][C:9]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][C:13]2=[O:18])=[CH:8][C:5]=1[C:6]#[N:7])([O-])=O>C1COCC1.[H][H].[Pd]>[NH2:1][C:4]1[CH:11]=[CH:10][C:9]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][C:13]2=[O:18])=[CH:8][C:5]=1[C:6]#[N:7]
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참가 물질

5

반응물 1

HCID 588264662-Nitro-5-(3-oxo-morpholin-4-yl)-benzonitrile

생성물 1

HCID 534164642-Amino-5-(3-oxo-morpholin-4-YL)-benzonitrile수율 60%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매HCID 178418361HCID 178418361, 화합물용매

실험 절차

2-Nitro-5-(3-oxo-morpholin-4-yl)-benzonitrile (1.1 g) was dissolved in THF (80 ml) and hydrogenated with hydrogen (1 atm) over Pd/C 10% (350 mg) for 18 h at 25° C. The reaction mixture was then filtered through decalite and precipitated (AcOEt/heptane) to yield 2-amino-5-(3-oxo-morpholin-4-yl)-benzonitrile as a white solid (580 mg). MH+=218.4

후처리

  1. filtrationThe reaction mixture was then filtered through decalite
  2. customprecipitated (AcOEt/heptane)

출처 및 근거

ORD 기록
ord-babec7680ff04e789b9bc3a12ed08238
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07601752B2

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