홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Dimethylformamide → 5-(4-methoxybenzoyl)-6-methyl-2(1H)-pyridinone

HRID 638196
노트
인쇄 미리보기

반응식

HRID 638196 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=[O:14])[CH:10]=[C:11]([CH3:13])[NH2:12])=[CH:5][CH:4]=1.CN(C)C=O.[C:20](OC)(=[O:23])[C:21]#[CH:22]>C(O)(C)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]([C:10]2[CH:22]=[CH:21][C:20](=[O:23])[NH:12][C:11]=2[CH3:13])=[O:14])=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 13536Methyl propiolateHCID 15171633-Amino-1-(4-methoxyphenyl)but-2-en-1-one

생성물 1

HCID 217799405-(4-methoxybenzoyl)-6-methyl-2(1H)-pyridinone

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

To a stirred solution containing 93 g of 3-(4-methoxyphenyl)-1-methyl-3-oxo-1-propenamine and 200 ml of dimethylformamide was added 46 ml of methyl propiolate over a 30 minute period and the reaction mixture was stirred at ambient temperature for 3 hours and then gently refluxed for 24 hours. The reaction mixture was allowed to cool, treated with 200 ml of isopropyl alcohol and the solid filtered. The solid was washed with isopropyl alcohol and dried at 90°-95° C. to yield, as white shiny crystals, 75.8 g of 5-(4-methoxybenzoyl)-6-methyl-2(1H)-pyridinone, m.p. 228°-230° C.

후처리

  1. temperaturegently refluxed for 24 hours
  2. temperatureto cool
  3. filtrationthe solid filtered
  4. washThe solid was washed with isopropyl alcohol
  5. customdried at 90°-95° C.

출처 및 근거

ORD 기록
ord-9f008ceff6224592b2d6e489be7d5cfd
출처 데이터셋
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04560691

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트