3,4-Dichloroaniline → HCID 21923095, 화합물

HRID 2233140노트

반응식

HRID 2233140 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[Cl:9])[NH2:5].Cl[C:11]1[N:16]=[C:15]([Cl:17])[C:14]([C:18]([F:21])([F:20])[F:19])=[CH:13][N:12]=1.C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1>[Cl:1][C:2]1[CH:3]=[C:4]([NH:5][C:11]2[N:16]=[C:15]([Cl:17])[C:14]([C:18]([F:20])([F:21])[F:19])=[CH:13][N:12]=2)[CH:6]=[CH:7][C:8]=1[Cl:9]

참가 물질

5

실험 절차

4.86 g of 3,4-dichloroaniline dissolved in 10 ml of dioxane are added to 6.51 g of 2,4-dichloro-5-trifluoromethyl-pyrimidine in 40 ml of dioxane at ambient temperature. Then 6 ml of 5 M potassium carbonate solution are added and the mixture is stirred for three days at ambient temperature. It is then filtered through Alox B (20 ml) and washed with dioxane. The filtrate is concentrated by evaporation, the residue dissolved in 50 ml methylene chloride and this solution is cooled in a bath of dry ice and acetone. The precipitate is suction filtered and the filtrate is cooled again. After suction filtering again the precipitates are combined and the filtrate is concentrated by evaporation. The residue is separated by chromatography through an RP18 column (gradient: acetonitrile: H2O=20:80 to 80:20).

후처리

  1. filtrationIt is then filtered through Alox B (20 ml)
  2. washwashed with dioxane
  3. concentrationThe filtrate is concentrated by evaporation
  4. dissolutionthe residue dissolved in 50 ml methylene chloride
  5. temperaturethis solution is cooled in a bath of dry ice and acetone
  6. filtrationfiltered
  7. temperaturethe filtrate is cooled again
  8. filtrationAfter suction filtering again the precipitates
  9. concentrationthe filtrate is concentrated by evaporation
  10. customThe residue is separated by chromatography through an RP18 column (gradient: acetonitrile: H2O=20:80 to 80:20)

출처 및 근거

ORD 기록
ord-3e43a8da401f4d568bb107c2963b0675
출처 데이터셋
uspto-grants-2010_05
특허 번호
US07709480B2

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