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Ammonium Chloride → 3-amino-1-(4-fluorophenyl)pyridin-2(1H)-one

HRID 1361415
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인쇄 미리보기

반응식

HRID 1361415 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:13]=[CH:12][CH:11]=[C:10]([N+:14]([O-])=O)[C:9]2=[O:17])=[CH:4][CH:3]=1.[Cl-].[NH4+]>C1COCC1.CO.CCOC(C)=O.[Zn]>[NH2:14][C:10]1[C:9](=[O:17])[N:8]([C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)[CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 2

HCID 25517Ammonium ChlorideHCID 58879966HCID 58879966, 화합물

생성물 1

HCID 588799723-amino-1-(4-fluorophenyl)pyridin-2(1H)-one수율 100%

시약·촉매·용매 4

HCID 23994Zinc촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 1-(4-fluorophenyl)-3-nitropyridin-2(1H)-one (610 mg, 2.6 mmol) in THF (50 mL) and MeOH (50 mL), were added ammonium chloride (695 mg, 13.0 mmol, EMD) and Zn dust (850 mg, 13.0 mmol, Aldrich). The reaction mixture was stirred at room temperature for 3 h, diluted with 200 mL of EtOAc and filtered through a pad of Celitee. The filtrate was concentrated in vacuo to give the desired product (530 mg, 100% yield) as a brown solid. MS(ESI+) m/z 205.29 (M+H)+.

후처리

  1. filtrationfiltered through a pad of Celitee
  2. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-435e13b1e9d94afe85eda32820002c28
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07880004B2

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 8857
Ethyl Acetate
용매