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Acetic Anhydride → N-[5-(5-Chloropyridin-3-ylethynyl)-2-fluorophenyl]-acetamide

HRID 606947
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인쇄 미리보기

반응식

HRID 606947 반응식
C(O[C:5](=[O:7])[CH3:6])(=O)C.[Cl:8][C:9]1[CH:10]=[C:11]([C:15]#[C:16][C:17]2[CH:18]=[CH:19][C:20]([F:24])=[C:21]([NH2:23])[CH:22]=2)[CH:12]=[N:13][CH:14]=1>N1C=CC=CC=1>[Cl:8][C:9]1[CH:10]=[C:11]([C:15]#[C:16][C:17]2[CH:18]=[CH:19][C:20]([F:24])=[C:21]([NH:23][C:5](=[O:7])[CH3:6])[CH:22]=2)[CH:12]=[N:13][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 670475245-(5-Chloropyridin-3-ylethynyl)-2-fluorophenylamine

생성물 1

HCID 67048115N-[5-(5-Chloropyridin-3-ylethynyl)-2-fluorophenyl]-acetamide수율 75%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Add acetic anhydride (113 mg, 1.11 mmol) to a solution of 5-(5-chloropyridin-3-ylethynyl)-2-fluorophenylamine, (prepared as described in EXAMPLE 190) (0.275 g, 1.11 mmol) in pyridine (4 mL). Stir the mixture at room temperature under nitrogen for 18 h then concentrate. Purify by silica gel chromatography, eluting with a gradient of 75:25 to 50:50 with hexanes:ethyl acetate, followed by a second silica gel chromatography, eluting with 75:25 to 60:40 hexanes:ethyl acetate, to give the title compound as a white solid (240 mg, 75%).

후처리

  1. concentrationthen concentrate
  2. customPurify by silica gel chromatography
  3. washeluting with a gradient of 75:25 to 50:50 with hexanes
  4. washeluting with 75:25 to 60:40 hexanes

출처 및 근거

ORD 기록
ord-05e52521de73499697351accedf92c96
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915424B2

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