Ammonia → 2-Butoxy-9-(3-bromopropyl)-7,8-dihydro-8-oxoadenine

HRID 1666199Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1666199
[Br:1][CH2:2][CH2:3][CH2:4][N:5]1[C:13]([O:14]C)=[N:12][C:11]2[C:6]1=[N:7][C:8]([O:17][CH2:18][CH2:19][CH2:20][CH3:21])=[N:9][C:10]=2[NH2:16].Cl.N>CO.O1CCOCC1>[CH2:18]([O:17][C:8]1[N:7]=[C:6]2[C:11]([NH:12][C:13](=[O:14])[N:5]2[CH2:4][CH2:3][CH2:2][Br:1])=[C:10]([NH2:16])[N:9]=1)[CH2:19][CH2:20][CH3:21]

Komponenten

6

Edukt 3

HCID 222AmmoniaHCID 313Hydrochloric AcidHCID 231584909-(3-Bromopropyl)-2-butoxy-8-methoxy-9H-purin-6-amine

Produkt 1

HCID 592880312-Butoxy-9-(3-bromopropyl)-7,8-dihydro-8-oxoadenineAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

To a solution of the compound (1 g, 2.79 mmol) obtained in Step (i) in methanol (2 ml) was added a 4N-hydrochloric acid in dioxane (2 ml), and the mixture was stirred at room temperature for 3.5 hours. The mixture was neutralized by addition of 28% aqueous ammonia at 0° C., and the mixture was stirred for one hour. The precipitated crystals were collected by filtration, washed twice with water (2 ml) and further washed twice with methanol (2 ml), and dried to give the subtitle compound (882 mg) as a white solid. Yield: 92%

Aufarbeitung

  1. stirringthe mixture was stirred for one hour
  2. filtrationThe precipitated crystals were collected by filtration
  3. washwashed twice with water (2 ml)
  4. washfurther washed twice with methanol (2 ml)
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-7481010a905a461d9e1c2415770efa28
Quelldatensatz
uspto-grants-2011_10
Patentnummer
US08044056B2

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