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Methylamine → N-Methyl-N-[(4-{[2-(trifluoromethyl)pyrimidin-5-yl]oxy}phenyl)methyl]amine

HRID 1926719
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인쇄 미리보기

반응식

HRID 1926719 반응식
[F:1][C:2]([F:19])([F:18])[C:3]1[N:8]=[CH:7][C:6]([O:9][C:10]2[CH:17]=[CH:16][C:13]([CH:14]=O)=[CH:12][CH:11]=2)=[CH:5][N:4]=1.[CH3:20][NH2:21]>C(O)C>[CH3:20][NH:21][CH2:14][C:13]1[CH:16]=[CH:17][C:10]([O:9][C:6]2[CH:5]=[N:4][C:3]([C:2]([F:19])([F:18])[F:1])=[N:8][CH:7]=2)=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329MethylamineHCID 866231314-{[2-(Trifluoromethyl)-5-pyrimidinyl]oxy}benzaldehyde

생성물 1

HCID 67131360N-Methyl-N-[(4-{[2-(trifluoromethyl)pyrimidin-5-yl]oxy}phenyl)methyl]amine수율 95%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4-{[2-(Trifluoromethyl)pyrimidin-5-yl]oxy}benzaldehyde was stirred with 33% methylamine in 95% ethanol (30 mL) at reflux for 1 hour and then concentrated. The residue was re-dissolved in 95% ethanol, 10% palladium/carbon was added, and the mixture was hydrogenated at room temperature under atmospheric pressure for 30 minutes. The reaction was performed on a 5.0 mmol scale with a yield of 95%.

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후처리

  1. temperatureat reflux for 1 hour
  2. concentrationconcentrated
  3. dissolutionThe residue was re-dissolved in 95% ethanol
  4. addition10% palladium/carbon was added

출처 및 근거

ORD 기록
ord-d96ceca2f1704177a97dbbdacbd3f42b
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08183251B2

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