Ammonia → 2-acetamido-N-(4-nitrophenyl)benzamide

HRID 1711365

Reaktionsgleichung

Reaktionsgleichung von HRID 1711365
N[C:2]1[CH:19]=[CH:18][C:5]([C:6]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][CH:10]=2)=[O:7])=[CH:4][CH:3]=1.NC1N=C(C)[CH:24]=[C:23](Cl)[N:22]=1.Cl.N.C([O:33]CCO)C>C(OCC)(=O)C.CO.O>[C:23]([NH:22][C:18]1[CH:19]=[CH:2][CH:3]=[CH:4][C:5]=1[C:6]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][CH:10]=1)=[O:7])(=[O:33])[CH3:24]

Komponenten

9

Edukt 5

HCID 222AmmoniaHCID 313Hydrochloric AcidHCID 8076Glycol monoethyl etherHCID 218102-Amino-4-chloro-6-methylpyrimidineHCID 30155604-Amino-4'-nitrobenzanilide

Produkt 1

HCID 33533142-acetamido-N-(4-nitrophenyl)benzamide

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

4-Amino-N-(4-nitrophenyl)benzamide (C1) (730 mg, 2.84 mmol) and 4-chloro-6-methyl-2-pyrimidinylamine (A8) (416 mg, 2.84 mmol) were dissolved in warm 2-ethoxyethanol (20 mL), two drops c.HCl was then added to the reaction mixture was refluxed for 40 min. by which time TLC and MS showed the completion of the reaction. The reaction mixture was diluted with ethyl acetate and cooled to 20° C. The resulting precipitate was filtered and washed with more EtOAc to give a solid product. This was suspended in MeOH and basified with aqueous NH3 and diluted with water. The resulting precipitate was filtered and dried to give C2 (671 mg). The filtrate was concentrated to give a further 276 mg of C2 (92% overall): mp (MeOH)>300° C.; 1H NMR [(CD3)2SO] δ 10.59 (s, 1H, NH), 9.37 (s, 1H, NH), 8.27-8.24 (m, 2H, ArH), 8.09-8.06 (m, 2H, ArH), 8.05-7.90 (m, 4H, ArH), 6.25 (s, 2H, NH2), 5.96 (s, 1H, ArH), 2.16 (s, 3 H, CH3); Mass APCl+365.

Aufarbeitung

  1. temperaturewas refluxed for 40 min. by which time TLC and MS
  2. customthe completion of the reaction
  3. filtrationThe resulting precipitate was filtered
  4. washwashed with more EtOAc
  5. customto give a solid product
  6. filtrationThe resulting precipitate was filtered
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-80a565a10bdf4867b4a4c52a5a6b8ff0
Quelldatensatz
uspto-grants-2010_09
Patentnummer
US07790746B2

Verknüpfte Notizen

Wird geladen…