4-tert-Butylbenzoyl chloride → HCID 86652256, Verbindung

HRID 1256280

Reaktionsgleichung

Reaktionsgleichung von HRID 1256280
[Cl:1][C:2]1[N:7]2[N:8]=[CH:9][CH:10]=[C:6]2[N:5]=[C:4]([NH2:11])[CH:3]=1.[Cl:12][C:13]1[N:18]2[N:19]=[C:20]([CH3:22])[CH:21]=[C:17]2[N:16]=[C:15]([NH2:23])[CH:14]=1.[C:24]([C:28]1[CH:36]=[CH:35][C:31]([C:32](Cl)=[O:33])=[CH:30][CH:29]=1)([CH3:27])([CH3:26])[CH3:25]>N1C=CC=CC=1>[C:24]([C:28]1[CH:29]=[CH:30][C:31]([C:32]([NH:11][C:4]2[CH:3]=[C:2]([Cl:1])[N:7]3[N:8]=[CH:9][CH:10]=[C:6]3[N:5]=2)=[O:33])=[CH:35][CH:36]=1)([CH3:27])([CH3:25])[CH3:26].[C:24]([C:28]1[CH:29]=[CH:30][C:31]([C:32]([NH:23][C:15]2[CH:14]=[C:13]([Cl:12])[N:18]3[N:19]=[C:20]([CH3:22])[CH:21]=[C:17]3[N:16]=2)=[O:33])=[CH:35][CH:36]=1)([CH3:27])([CH3:25])[CH3:26]

Komponenten

6

Edukt 3

HCID 743724-tert-Butylbenzoyl chlorideHCID 442513067-Chloropyrazolo[1,5-a]pyrimidin-5-amineHCID 442513077-Chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-amine

Produkt 2

HCID 86652256HCID 86652256, VerbindungAusbeute 47 %HCID 86652257HCID 86652257, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

7-Chloropyrazolo[1,5-a]pyrimidin-5-amine 1E (1.0 equivalent) or 7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-amine (1J, 1.0 equivalent) was dissolved in anhydrous pyridine (0.35 M). 4-t-Butylbenzoic acid chloride (1.05 equivalents) was added at 0° C., and the mixture was stirred for two hours. The reaction was then quenched with saturated NaHCO3; pyridine was removed in vacuo and the residue was extracted with EtOAc. Combined organic layers were washed twice with 0.2 N HCl to remove residual pyridine, dried over MgSO4, filtered and concentrated. Crude product was purified by column chromatography (SiO2, gradient of 15 to 30% EtOAc/hexanes). The purified product was triturated with Et2O to give 4-tert-butyl-N-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)benzamide (1F, 47%) or 4-tert-butyl-N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)benzamide (1K) of the product as a solid.

Aufarbeitung

  1. customThe reaction was then quenched with saturated NaHCO3
  2. custompyridine was removed in vacuo
  3. extractionthe residue was extracted with EtOAc
  4. washCombined organic layers were washed twice with 0.2 N HCl
  5. customto remove residual pyridine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customCrude product was purified by column chromatography (SiO2, gradient of 15 to 30% EtOAc/hexanes)
  10. customThe purified product was triturated with Et2O

Quellen und Nachweise

ORD-Eintrag
ord-ffcfe71dd2c245f288db32593ab7ca2f
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08461163B2

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