4-Aminophenol → 2-Amino-5-(4-chlorophenoxy)-4-(4-hydroxyanilino)pyrimidine hydrochloride

HRID 895395

Reaktionsgleichung

Reaktionsgleichung von HRID 895395
[Cl:1][C:2]1[C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][CH:10]=2)=[CH:6][N:5]=[C:4]([N:16]=CN(C(C)C)C(C)C)[N:3]=1.[NH2:25][C:26]1[CH:31]=[CH:30][C:29]([OH:32])=[CH:28][CH:27]=1>CO>[ClH:1].[NH2:16][C:4]1[N:3]=[C:2]([NH:25][C:26]2[CH:31]=[CH:30][C:29]([OH:32])=[CH:28][CH:27]=2)[C:7]([O:8][C:9]2[CH:10]=[CH:11][C:12]([Cl:15])=[CH:13][CH:14]=2)=[CH:6][N:5]=1

Komponenten

4

Edukt 2

HCID 4034-AminophenolHCID 540285984-Chloro-5-(4-chlorophenoxy)-2-(diisopropylaminomethyleneamino)pyrimidine

Produkt 1

HCID 223803932-Amino-5-(4-chlorophenoxy)-4-(4-hydroxyanilino)pyrimidine hydrochlorideAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
24 °C

Versuchsvorschrift

Nitrogen was bubbled through a suspension of 10.11 g (27.5 mmol) of 4-chloro-5-(4-chlorophenoxy)-2-(diisopropylaminomethyleneamino)pyrimidine (see Example 2) in 205 ml of methanol for 10 minutes. Then 3.18 g (29.1 mmol) of 4-aminophenol was added and nitrogen bubbled through the suspension for 5 minutes. The solution was then tightly sealed and stirred at 24° C. for 20 hours. Then 50 ml of concentrated hydrochloric acid was added to the mixture and refluxed for 140 minutes. The mixture was cooled and spin evaporated to one-half the original volume and then stored at 3° C. After 3 hours, a large precipitate had formed which was collected by filtration and washed quickly with cold methanol. The filter cake was suspended in 79 ml of CH2Cl2 and the suspension was boiled for 5 minutes. The solids were collected by filtration, washed with CH2Cl2 and dried in vacuo at 100° C. 8.6 g (86%) of product as a pale yellow powder was obtained, mp 288-289° C.

Aufarbeitung

  1. customnitrogen bubbled through the suspension for 5 minutes
  2. customThe solution was then tightly sealed
  3. additionThen 50 ml of concentrated hydrochloric acid was added to the mixture
  4. temperaturerefluxed for 140 minutes
  5. temperatureThe mixture was cooled
  6. customspin evaporated to one-half the original volume
  7. customstored at 3° C
  8. waitAfter 3 hours
  9. customa large precipitate had formed which
  10. filtrationwas collected by filtration
  11. washwashed quickly with cold methanol
  12. waitthe suspension was boiled for 5 minutes
  13. filtrationThe solids were collected by filtration
  14. washwashed with CH2Cl2
  15. customdried in vacuo at 100° C

Quellen und Nachweise

ORD-Eintrag
ord-b8d337e1c38d48cd86cf38bb542d24e3
Quelldatensatz
uspto-grants-2005_07
Patentnummer
US06916820B1

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