Triethylamine → 3-[5-chloro-4-(3-methoxy-benzyloxy)-2-methyl-6-oxo-6H-pyrimidin-1-yl]-N-methoxy-4,N-dimethyl-benzamide

HRID 2172609Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2172609
[Cl:1][C:2]1[C:7](=[O:8])[N:6]([C:9]2[CH:10]=[C:11]([CH:15]=[CH:16][C:17]=2[CH3:18])[C:12](O)=[O:13])[C:5]([CH3:19])=[N:4][C:3]=1[O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([O:28][CH3:29])[CH:23]=1.[C:30](N1C=CN=C1)(N1C=CN=C1)=O.Cl.[CH3:43][N:44](C)[OH:45].C(N(CC)CC)C>O1CCCC1>[Cl:1][C:2]1[C:7](=[O:8])[N:6]([C:9]2[CH:10]=[C:11]([CH:15]=[CH:16][C:17]=2[CH3:18])[C:12]([N:44]([O:45][CH3:30])[CH3:43])=[O:13])[C:5]([CH3:19])=[N:4][C:3]=1[O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([O:28][CH3:29])[CH:23]=1

Komponenten

6

Versuchsvorschrift

To a solution of 3-[5-chloro-4-(3-methoxy-benzyloxy)-2-methyl-6-oxo-6H-pyrimidin-1-yl]-4-methyl-benzoic acid from step C (230 mg, 0.56 mmol) in tetrahydrofuran (2 mL) was added 1,1′-carbonyldiimidazole (135 mg, 0.83 mmol). After stirring at ambient temperature for three hours, N,N-dimethylhydroxylamine HCl (80 mg, 0.83 mmol) and triethylamine (0.15 mL, 1.12 mmol) were added. The solution continued to stir for eighteen hours. The solution was partitioned between ethyl acetate and water. The organic layer was washed with saturated sodium bicarbonate, water, 5% citric acid and brine and dried over magnesium sulfate. The slurry was filtered and concentrated to provide the amide as a light green oil (200 mg, 78%). MS (M+H): 458

Aufarbeitung

  1. stirringto stir for eighteen hours
  2. customThe solution was partitioned between ethyl acetate and water
  3. washThe organic layer was washed with saturated sodium bicarbonate, water, 5% citric acid and brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationThe slurry was filtered
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-a3a21df2449146c5b91de41cc724c2f2
Quelldatensatz
uspto-grants-2015_06
Patentnummer
US09056110B2

Notizen zur Reaktion

Wird geladen…