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Dimethylformamide dimethyl acetal → N-[[2-chloro-5-[3-(dimethylamino)-1-oxo-2-propen-1-yl]-phenyl]methyl]acetamide

HRID 1408419
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인쇄 미리보기

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HRID 1408419 반응식
[C:1]([C:4]1[CH:5]=[CH:6][C:7]([Cl:15])=[C:8]([CH2:10][NH:11][C:12](=[O:14])[CH3:13])[CH:9]=1)(=[O:3])[CH3:2].CO[CH:18](OC)[N:19]([CH3:21])[CH3:20]>C1(C)C=CC=CC=1>[Cl:15][C:7]1[CH:6]=[CH:5][C:4]([C:1](=[O:3])[CH:2]=[CH:18][N:19]([CH3:21])[CH3:20])=[CH:9][C:8]=1[CH2:10][NH:11][C:12](=[O:14])[CH3:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 11858678N-[(5-acetyl-2-chlorophenyl)methyl]acetamide

생성물 1

HCID 67151137N-[[2-chloro-5-[3-(dimethylamino)-1-oxo-2-propen-1-yl]-phenyl]methyl]acetamide

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
105 °C

실험 절차

A mixture of N-[(5-acetyl-2-chlorophenyl)methyl]acetamide (13.0 g, 57.8 mmol; prepared according to a procedure described in EP 1586552-A1) and N,N-dimethylformamide dimethyl acetal (13.8 g, 115.8 mmol) in toluene (130 mL) was heated at 105° C. overnight. The reaction mixture was then concentrated, and the resulting solid was washed with diethyl ether and n-pentane to yield the title product as a solid (10.0 g).

후처리

  1. customprepared
  2. concentrationThe reaction mixture was then concentrated
  3. washthe resulting solid was washed with diethyl ether and n-pentane

출처 및 근거

ORD 기록
ord-638fa86b8c2049dcb3c4ce048d34aad4
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921360B2

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