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Hydrochloric Acid → (6-Morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-carbamic acid methyl ester

HRID 379428
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 379428
[CH3:1][O-:2].[Na+].Br[N:5]1[C:9](=[O:10])CCC1=O.[N:12]1([C:18]2[CH:26]=[C:25]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=3[CH3:33])[C:21](C(N)=O)=[CH:20][N:19]=2)[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.Cl>ClCCl>[CH3:1][O:2][C:9](=[O:10])[NH:5][C:21]1[CH:20]=[N:19][C:18]([N:12]2[CH2:13][CH2:14][O:15][CH2:16][CH2:17]2)=[CH:26][C:25]=1[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[CH3:33]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 67184N-bromobutanimideHCID 10942334Sodium MethoxideHCID 111622966-Morpholin-4-yl-4-o-tolyl-nicotinamide

Produkt 1

HCID 12167319(6-Morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-carbamic acid methyl esterAusbeute 74,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344
Dichloromethane
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
-5 °C

Versuchsvorschrift

9.9 ml (53.7 mMol) Sodium methoxide solution (5.4 M in MeOH) were added over 15 minutes to a solution of 3.9 g (21.5 mMol) N-bromosuccinimide in 22.5 ml dichloromethane cooled to −5° C. The milky suspension was stirred at −5° C. for 18 hours, then, at the same temperature, a solution of 4.5 g (14 mMol) 6-morpholin-4-yl-4-o-tolyl-nicotinamide in 22.5 ml dichloromethane was added over 15 minutes. After 5 hours at 5° C., 33 ml (33 mMol) aqueous HCl 1N were added, the phases were separated, the organic phase washed with water and the aqueous phases extracted with dichloromethane. The combined organic phases were dried (Na2SO4) and evaporated. The residue was treated with basic Alox (1:1 weight) in ethyl acetate/heptane 1:1 for 30 minutes at room temperature. After filtration and removal of the solvents, the residue was crystallized from di-iso-propylether/n-heptane 1:2 at OOC to yield 3.4 g (72.5%) (6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-carbamic acid methyl ester as a yellow powder.

Aufarbeitung

  1. waitAfter 5 hours at 5° C.
  2. customthe phases were separated
  3. washthe organic phase washed with water
  4. extractionthe aqueous phases extracted with dichloromethane
  5. dry with materialThe combined organic phases were dried (Na2SO4)
  6. customevaporated
  7. additionThe residue was treated with basic Alox (1:1 weight) in ethyl acetate/heptane 1:1 for 30 minutes at room temperature
  8. filtrationAfter filtration and removal of the solvents
  9. customthe residue was crystallized from di-iso-propylether/n-heptane 1:2 at OOC

Quellen und Nachweise

ORD-Eintrag
ord-f8240ee793634f53981c04886dbd4be6
Quelldatensatz
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06297375B1

Notizen zur Reaktion

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