Tributylstannane → 4-Chloro-2-(tributylstannyl)pyrimidine

HRID 1529288Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1529288
[Li+].CC([N-]C(C)C)C.[SnH:9]([CH2:18][CH2:19][CH2:20][CH3:21])([CH2:14][CH2:15][CH2:16][CH3:17])[CH2:10][CH2:11][CH2:12][CH3:13].[Cl:22][C:23]1[N:28]=[C:27]([Cl:29])[CH:26]=[CH:25][N:24]=1>C1COCC1>[Cl:29][C:27]1[CH:26]=[CH:25][N:24]=[C:23]([Sn:9]([CH2:14][CH2:15][CH2:16][CH3:17])([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:10][CH2:11][CH2:12][CH3:13])[N:28]=1.[Cl:22][C:23]1[N:28]=[C:27]([Sn:9]([CH2:14][CH2:15][CH2:16][CH3:17])([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:10][CH2:11][CH2:12][CH3:13])[CH:26]=[CH:25][N:24]=1

Komponenten

6

Edukt 3

HCID 5948TributylstannaneHCID 775312,4-DichloropyrimidineHCID 2724682Lithium diisopropylamide

Produkt 2

HCID 149763044-Chloro-2-(tributylstannyl)pyrimidineAusbeute 24 %HCID 468399532-Chloro-4-(tributylstannyl)pyrimidineAusbeute 5,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a mixture of THF (300 mL) and LDA (100 mL, 20.1 mmol) at −20° C. was added SnBu3H (50 mL, 17.4 mmol) dropwise and stirred for 15 min. The reaction mixture was cooled to −78° C. and treated with 2,4-dichloro pyrimidine (20 g, 134 mmol) portionwise. The reaction mixture was stirred at −78° C. for 5 h with constant stirring under argon atmosphere. The cooling bath was removed and the reaction mixture was warmed up to 0° C. within 30 min. The resulting mixture was poured into 10% NH4Cl aqueous solution, and extracted the compound with Et2O. The organic layer was washed with brine, dried with Na2SO4, filtered, and evaporated. The residue was purified by column chromatography (1% EtOAc: 99% n-Hexane) to obtain 4-Chloro-2-tributylstannanyl-pyrimidine (13 g, 24% yield) as a pale yellow color syrup and 2-Chloro-4-tributylstannanyl-pyrimidine 20a (3 g, 5.5% yield) as a pale yellow color syrup.

Aufarbeitung

  1. stirringThe reaction mixture was stirred at −78° C. for 5 h
  2. stirringwith constant stirring under argon atmosphere
  3. customThe cooling bath was removed
  4. temperaturethe reaction mixture was warmed up to 0° C. within 30 min
  5. additionThe resulting mixture was poured into 10% NH4Cl aqueous solution
  6. extractionextracted the compound with Et2O
  7. washThe organic layer was washed with brine
  8. dry with materialdried with Na2SO4
  9. filtrationfiltered
  10. customevaporated
  11. customThe residue was purified by column chromatography (1% EtOAc: 99% n-Hexane)

Quellen und Nachweise

ORD-Eintrag
ord-aedd68e1cb7f4d10a54253a5dd562797
Quelldatensatz
uspto-grants-2015_07
Patentnummer
US09090593B2

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