StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Tetrahydrofuran → 5-Bromo-N-(pyrimidin-4-YL)-N-((2-(trimethylsilyl)ethoxy)methyl)naphthalene-2-sulfonamide

HRID 1473364
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1473364
[N:1]1[CH:6]=[CH:5][C:4]([NH2:7])=[N:3][CH:2]=1.[CH3:8][Si:9]([CH2:12][CH2:13][O:14][CH2:15]Cl)([CH3:11])[CH3:10].[Br:17][C:18]1[CH:27]=[CH:26][CH:25]=[C:24]2[C:19]=1[CH:20]=[CH:21][C:22]([S:28](OC1C(F)=C(F)C(F)=C(F)C=1F)(=[O:30])=[O:29])=[CH:23]2.CC(C)([O-])C.[Li+].C1COCC1>CN(C=O)C>[Br:17][C:18]1[CH:27]=[CH:26][CH:25]=[C:24]2[C:19]=1[CH:20]=[CH:21][C:22]([S:28]([N:7]([C:4]1[CH:5]=[CH:6][N:1]=[CH:2][N:3]=1)[CH2:15][O:14][CH2:13][CH2:12][Si:9]([CH3:11])([CH3:10])[CH3:8])(=[O:29])=[O:30])=[CH:23]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 8028TetrahydrofuranHCID 689584-AminopyrimidineHCID 27242712-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 236647642-Propanol, 2-methyl-, lithium salt (1:1)HCID 86687354Perfluorophenyl 5-bromonaphthalene-2-sulfonate2×

Produkt 1

HCID 86687411
5-Bromo-N-(pyrimidin-4-YL)-N-((2-(trimethylsilyl)ethoxy)methyl)naphthalene-2-sulfonamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A solution of pyrimidin-4-amine (0.944 g, 9.93 mmol) in 10 mL DMF was treated with SEM-Cl (1.761 ml, 9.93 mmol) and was allowed to stir at room temperature 30 minutes. Perfluorophenyl 5-bromonaphthalene-2-sulfonate (INTERMEDIATE M; 4.50 g, 9.93 mmol) was added and the reaction mixture was treated with lithium tert-butoxide 1N in THF (19.86 ml, 19.86 mmol) drop wise. After stirring for one hour, the reaction mixture was concentrated. The crude residue was diluted with DCM, washed with water, the organics dried over MgSO4 and concentrated. The material (INTERMEDIATE CCC) was carried forward crude without further purification.

Aufarbeitung

  1. stirringAfter stirring for one hour
  2. concentrationthe reaction mixture was concentrated
  3. additionThe crude residue was diluted with DCM
  4. washwashed with water
  5. dry with materialthe organics dried over MgSO4
  6. concentrationconcentrated
  7. customwithout further purification

Quellen und Nachweise

ORD-Eintrag
ord-ced9276fac1948328149ad3fe9cf87f4
Quelldatensatz
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09012443B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion