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Tetrahydrofuran → 6-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperazinyl]-ethyl]-2,3-dihydro-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one

HRID 2051020
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2051020
F[C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9](=[N:29][OH:30])[N:10]1[CH2:15][CH2:14][N:13]([CH2:16][CH2:17][C:18]2[C:23](=[O:24])[N:22]3[CH2:25][CH2:26][S:27][C:21]3=[N:20][C:19]=2[CH3:28])[CH2:12][CH2:11]1.O1CCCC1.[H-].[Na+].[OH-].[NH4+]>C(O)(=O)C.C(O)C.CC1C=CC=CC=1>[F:8][C:6]1[CH:5]=[CH:4][C:3]2[C:9]([N:10]3[CH2:15][CH2:14][N:13]([CH2:16][CH2:17][C:18]4[C:23](=[O:24])[N:22]5[CH2:25][CH2:26][S:27][C:21]5=[N:20][C:19]=4[CH3:28])[CH2:12][CH2:11]3)=[N:29][O:30][C:2]=2[CH:7]=1
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Komponenten

8

Edukt 4

HCID 8028TetrahydrofuranHCID 14923Ammonium HydroxideHCID 24758Sodium hydrideHCID 542159526-[2-[4-[(2,4-difluorophenyl)(hydroxyimino)methyl]-1-piperazinyl]ethyl]-2,3-dihydro-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one

Produkt 1

HCID 150574626-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperazinyl]-ethyl]-2,3-dihydro-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one
Ausbeute 91,4 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 176Acetic AcidLösungsmittelHCID 702EthanolLösungsmittelHCID 1140TolueneLösungsmittel

Versuchsvorschrift

A solution of 4.4 parts of 6-[2-[4-[(2,4-difluorophenyl)(hydroxyimino)methyl]-1-piperazinyl]ethyl]-2,3-dihydro-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one in 45 parts of tetrahydrofuran was stirred at room temperature. 0.5 Parts of a sodium hydride dispersion 50% were added portionwise. Upon complete addition, 108 parts of methylbenzene were added and the reaction mixture was stirred for 18 hours at reflux temperature. After cooling, 16 parts of ethanol were added, followed by the addition of 3 parts of acetic acid. The whole was stirred for 10 minutes. The mixture was treated with ammonium hydroxide and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 3.8 parts (91.4%) of 6-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperazinyl]-ethyl]-2,3-dihydro-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one; mp. 193.0° C. (compound 3).

Aufarbeitung

  1. additionwere added
  2. temperatureat reflux temperature
  3. temperatureAfter cooling
  4. stirringThe whole was stirred for 10 minutes
  5. extractionthe product was extracted with 4-methyl-2-pentanone
  6. customThe extract was dried
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue was purified by column chromatography over silica gel using
  10. additiona mixture of trichloromethane and methanol (95:5 by volume) as eluent
  11. customThe pure fractions were collected
  12. customthe eluent was evaporated
  13. customThe residue was crystallized from acetonitrile
  14. filtrationThe product was filtered off
  15. customdried

Quellen und Nachweise

ORD-Eintrag
ord-6932aa6853d9462885c8668d5f0a27a3
Quelldatensatz
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05015740

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