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Acetic Anhydride → N-[3-(7-Methyl-1,2,4-triazolo[4,3-b]pyridazin-6-yl)phenyl]acetamide

HRID 1763576
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반응식

HRID 1763576 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([C:8]2[C:9]([CH3:17])=[CH:10][C:11]3[N:12]([CH:14]=[N:15][N:16]=3)[N:13]=2)[CH:5]=[CH:6][CH:7]=1.[C:18](OC(=O)C)(=[O:20])[CH3:19]>N1C=CC=CC=1>[CH3:17][C:9]1[C:8]([C:4]2[CH:3]=[C:2]([CH:7]=[CH:6][CH:5]=2)[NH:1][C:18](=[O:20])[CH3:19])=[N:13][N:12]2[CH:14]=[N:15][N:16]=[C:11]2[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 22768927HCID 22768927, 화합물

생성물 1

HCID 20310384N-[3-(7-Methyl-1,2,4-triazolo[4,3-b]pyridazin-6-yl)phenyl]acetamide

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A 1.5 g. portion of 6-(m-aminophenyl)-7-methyl-1,2,4-triazolo[4,3-b]pyridazine (prepared as in Example 6) is dissolved in 30 ml. of pyridine at room temperature. To the solution is added 6.0 ml. of acetic anhydride and the reaction mixture is heated on a steam bath for 1 hour. The reaction mixture is cooled in an ice bath and is filtered. The filter cake is washed with petroleum ether and is dried to afford the product of the example as cream colored crystals, m.p. 298°-301° C.

후처리

  1. customat room temperature
  2. additionTo the solution is added 6.0 ml
  3. temperatureThe reaction mixture is cooled in an ice bath
  4. filtrationis filtered
  5. washThe filter cake is washed with petroleum ether
  6. customis dried
  7. customto afford the product of the example as cream colored crystals, m.p. 298°-301° C.

출처 및 근거

ORD 기록
ord-76dfc698c7224d01974f68ab28134729
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04112095

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