Dimethylformamide → 2-[1-(4-chlorophenyl)cyclobutyl]-N-[1-oxo-4-(trifluoromethyl)phthalazin-2(1H)-yl]acetamide

HRID 469557

Reaktionsgleichung

Reaktionsgleichung von HRID 469557
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([C:12](=O)[CH:13]=[N+:14]=[N-:15])[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.NN1[N:27]=[C:26]([C:28]([F:31])([F:30])[F:29])[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[C:19]1=[O:32].C(N(CC)CC)C.CN(C=[O:44])C>CCOC(C)=O.C([O-])(=O)C1C=CC=CC=1.[Ag+]>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([CH2:12][C:13]([NH:14][N:15]3[N:27]=[C:26]([C:28]([F:31])([F:30])[F:29])[C:25]4[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=4)[C:19]3=[O:32])=[O:44])[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1

Komponenten

7

Versuchsvorschrift

A solution of the above crude 1-(1-(4-chlorophenyl)cyclobutyl)-2-diazoethanone (65.6 mg, 0.280 mmol), the product from Example 11B (0.0503 g, 0.219 mmol), triethylamine (0.12 mL, 0.86 mmol), and silver benzoate (12.4 mg, 0.054 mmol) in DMF (1 mL) was stirred for 2 hours, diluted with EtOAc, washed with saturated aqueous NaHCO3 and brine, dried (Na2SO4), and filtered. The residue was chromatographed on SiO2 (4% EtOAc/dichloromethane) to give the title compound (33.5 mg) as a white solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 11.50 (s, 1H), 8.41 (dd, J=7.9, 1.4 Hz, 1H), 8.09-8.15 (m, 1H), 8.02-8.07 (m, 1H), 7.97-8.02 (m, 1H), 7.30-7.34 (m, 2H), 7.21-7.24 (m, 2H), 2.80 (s, 2H), 2.44-2.49 (m, 2H), 2.26-2.39 (m, 2H), 2.06-2.21 (m, 1H), 1.70-1.84 (m, 1H); MS (ESI+) M/Z 436 (M+H)+.

Aufarbeitung

  1. washwashed with saturated aqueous NaHCO3 and brine
  2. dry with materialdried (Na2SO4)
  3. filtrationfiltered
  4. customThe residue was chromatographed on SiO2 (4% EtOAc/dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-67c07523bd4245a294c12a19b76207f6
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08629143B2

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