Methanol → Isopropyl 5-(2-aminoethoxymethyl)-3-cyano-7-(2,3-difluorophenyl)-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carboxylate hydrochloride

HRID 2073627Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2073627
[C:1]([C:3]1[CH:4]=[N:5][N:6]2[CH:11]([C:12]3[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[C:13]=3[F:19])[C:10]([C:20]([O:22][CH:23]([CH3:25])[CH3:24])=[O:21])=[C:9]([CH2:26][O:27][CH2:28][CH2:29][N:30]3C(=O)C4=CC=CC=C4C3=O)[NH:8][C:7]=12)#[N:2].CO.O.NN.C(Cl)(Cl)[Cl:47]>>[ClH:47].[NH2:30][CH2:29][CH2:28][O:27][CH2:26][C:9]1[NH:8][C:7]2[N:6]([N:5]=[CH:4][C:3]=2[C:1]#[N:2])[CH:11]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[C:13]=2[F:19])[C:10]=1[C:20]([O:22][CH:23]([CH3:25])[CH3:24])=[O:21]

Komponenten

5

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a solution of 1.3 g of isopropyl 3-cyano-7-(2,3-difluorophenyl)-5-[2-(phthalimido)ethoxymethyl]-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carboxylate in a mixed solvent of 12 ml of methanol and 12 ml of chloroform is added 142 μl of hydrazine hydrate and the mixture is refluxed at 50° C. for 5 hours. After the solvent is distilled off, to the residue is added aqueous sodium hydrogencarbonate and then extracted with ethyl acetate. The organic layer is washed with water, dried over sodium sulfate and ethanolic hydrochloric acid is added to convert into hydrochloride. The obtained crystals are recrystallized from methanol to give 0.4 g of isopropyl 5-(2-aminoethoxymethyl)-3-cyano-7-(2,3-difluorophenyl)-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carboxylate hydrochloride 1/4 hydrate.

Aufarbeitung

  1. distillationAfter the solvent is distilled off, to the residue
  2. additionis added aqueous sodium hydrogencarbonate
  3. extractionextracted with ethyl acetate
  4. washThe organic layer is washed with water
  5. dry with materialdried over sodium sulfate and ethanolic hydrochloric acid
  6. additionis added
  7. customThe obtained crystals are recrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-a0ec6ba8946e4a8888c856c1fd9ec0c4
Quelldatensatz
uspto-grants-1990_04
Patentnummer
US04918074

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