Water → 3-(2,6-Dichloro-3,5-dimethoxy-phenyl)-1-[6-(2-nitro-phenylamino)pyrimidin-4-yl]1-pyridin-3-ylmethyl-urea

HRID 58131Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 58131
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][C:11]1[CH:16]=[C:15]([NH:17][CH2:18][C:19]2[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=2)[N:14]=[CH:13][N:12]=1)([O-:3])=[O:2].[H-].[Na+].[Cl:27][C:28]1[C:33]([N:34]=[C:35]=[O:36])=[C:32]([Cl:37])[C:31]([O:38][CH3:39])=[CH:30][C:29]=1[O:40][CH3:41].O>C1COCC1>[Cl:27][C:28]1[C:29]([O:40][CH3:41])=[CH:30][C:31]([O:38][CH3:39])=[C:32]([Cl:37])[C:33]=1[NH:34][C:35](=[O:36])[N:17]([C:15]1[CH:16]=[C:11]([NH:10][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N+:1]([O-:3])=[O:2])[N:12]=[CH:13][N:14]=1)[CH2:18][C:19]1[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=1

Komponenten

6

Versuchsvorschrift

To a solution of N-(2-nitro-phenyl)-N′-pyridin-3-ylmethyl-pyrimidine-4,6-diamine (150 g, 0.467 mmol) in THF (15 mL) was added NaH (60%, 48 g, 1.2 mmol) at 0° C., and the mixture was stirred for 30 minutes at room temperature. A solution of 2,4-dichloro-3-isocyanato-1,5-dimethoxy-benzene (procedure 2A, steps a-d; 180 g, 0.73 mmol) was added dropwise at room temperature. The resulting mixture was stirred for 2 hours. Water (2 mL) was added to quench the reaction. The mixture was concentrated, and the residue was purified by flash chromatography on silica to obtain the title compound (85 mg, yield: 32%). MS (ESI): 570 [M+H]+.

Aufarbeitung

  1. stirringThe resulting mixture was stirred for 2 hours
  2. customto quench
  3. customthe reaction
  4. concentrationThe mixture was concentrated
  5. customthe residue was purified by flash chromatography on silica

Quellen und Nachweise

ORD-Eintrag
ord-4257a1978a544079a17cda17ca187a4e
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09434697B2

Notizen zur Reaktion

Wird geladen…