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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 5-(5-Bromo-2-chloropyrimidin-4-yl)-N-(4-fluorophenyl)thiazol-2-amine

HRID 2267390
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2267390
[Li]C(C)(C)C.[F:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][C:14]2[S:15][CH:16]=[CH:17][N:18]=2)=[CH:9][CH:8]=1.[Br:19][C:20]1[CH:21]=[N:22][C:23]([Cl:26])=[N:24][CH:25]=1.ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl.O=C1O[C@H]([C@H](CO)O)C([O-])=C1O.[Na+]>CCCCCCC.C1COCC1.O.CO>[Br:19][C:20]1[C:21]([C:16]2[S:15][C:14]([NH:13][C:10]3[CH:9]=[CH:8][C:7]([F:6])=[CH:12][CH:11]=3)=[N:18][CH:17]=2)=[N:22][C:23]([Cl:26])=[N:24][CH:25]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 5

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6066655-Bromo-2-chloropyrimidineHCID 23667548Sodium AscorbateHCID 25093329N-(4-Fluorophenyl)thiazol-2-amineHCID 178418306HCID 178418306, Verbindung

Produkt 1

HCID 60204511
5-(5-Bromo-2-chloropyrimidin-4-yl)-N-(4-fluorophenyl)thiazol-2-amine

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittelHCID 8028TetrahydrofuranLösungsmittelHCID 8900HeptaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

8.1 mL (12 mmol) of a 1.5 M solution of tBuLi in heptane was added to a stirred solution of 1.1 g (5.5 mmol) of N-(4-fluorophenyl)thiazol-2-amine in 20 mL of THF at −20° C. The solution was stirred for 30 min and then cooled to −78° C. before 1.3 g (6.6 mmol) of 5-bromo-2-chloropyrimidine was added. The reaction solution was stirred for 30 min at −78° C., then quenched by addition of 0.2 mL of AcOH in 1 mL of MeOH. Solid 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (10.4 g, 46 mmol) and 5 mL of MeOH were added and the reaction solution was warmed to 0° C. and stirred for 30 min, poured into 50 mL of a 0.5 M solution of sodium ascorbate, diluted with 200 mL of water and the crude product removed by filtration and washed repeatedly with water. The crude product was purified by flash chromatography eluting with a linear gradient of 10% EtOAc in hexane to 80% EtOAc in hexane to deliver the desired compound. MS (M+H)+ 387.

Aufarbeitung

  1. additionwas added
  2. stirringThe reaction solution was stirred for 30 min at −78° C.
  3. customquenched by addition of 0.2 mL of AcOH in 1 mL of MeOH
  4. stirringstirred for 30 min
  5. customthe crude product removed by filtration
  6. washwashed repeatedly with water
  7. customThe crude product was purified by flash chromatography
  8. washeluting with a linear gradient of 10% EtOAc in hexane to 80% EtOAc in hexane

Quellen und Nachweise

ORD-Eintrag
ord-b8f23b23c71a4e7abbe33b856fc0c3df
Quelldatensatz
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07858785B2

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