Carbon Dioxide → N-(2-dimethylaminoethyl)-2-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)propionamide

HRID 51498Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 51498
[NH2:1][C:2]1[C:3]2[C:10]([C:11]3[CH:16]=[CH:15][C:14]([O:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)=[CH:13][CH:12]=3)=[CH:9][N:8]([CH:24]([CH3:30])[C:25](OCC)=[O:26])[C:4]=2[N:5]=[CH:6][N:7]=1.[CH3:31][N:32]([CH3:36])[CH2:33][CH2:34][NH2:35].C(=O)=O>CO>[CH3:31][N:32]([CH3:36])[CH2:33][CH2:34][NH:35][C:25](=[O:26])[CH:24]([N:8]1[C:4]2[N:5]=[CH:6][N:7]=[C:2]([NH2:1])[C:3]=2[C:10]([C:11]2[CH:12]=[CH:13][C:14]([O:17][C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)=[CH:15][CH:16]=2)=[CH:9]1)[CH3:30]

Komponenten

5

Versuchsvorschrift

A mixture of ethyl 2-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]propionate (425 mg), N,N-dimethylethylenediamine (2 ml) and methanol (20 ml) was boiled under reflux for 18 hours with the exclusion of carbon dioxide. The mixture was cooled and filtered, the filtrate was diluted with water (50 ml) and stirred with ether. The mixture was left standing for 18 hours and the solid which precipitated was collected by filtration, washed with water and then ether and dried to give N-(2-dimethylaminoethyl)-2-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)propionamide, m.p. 163-164° C.

Aufarbeitung

  1. temperatureThe mixture was cooled
  2. filtrationfiltered
  3. additionthe filtrate was diluted with water (50 ml)
  4. waitThe mixture was left
  5. customthe solid which precipitated
  6. filtrationwas collected by filtration
  7. washwashed with water
  8. dry with materialether and dried

Quellen und Nachweise

ORD-Eintrag
ord-491ecddd74694791a56ba0b52cd34afe
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06713474B2

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