تفاعل #314297

ord-ead8bca681e14c00af7fb6607962ec01

معادلة التفاعل

NC(=O)C(F)(F)F
trifluoroacetamide
Cc1ccc(C(=O)c2c[nH]c3ccccc3c2=O)nc1C
3-(5,6-dimethyl-pyridine-2-carbonyl)-1H-quinolin-4-one
[H-].[Na+]
sodium hydride
O=C(Nc1cccc(CBr)n1)C(F)(F)F
N-(6-bromomethyl-pyridin-2-yl)-2,2,2-trifluoro-acetamide
Cc1ccc(C(=O)c2cn(Cc3cccc(N)n3)c3ccccc3c2=O)nc1C
1-(6-Amino-pyridin-2-ylmethyl)-3-(5,6-dimethyl-pyridine-2-carbonyl)-1H-quinolin-4-one

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىovernight
  2. 2
    أخرىat 45° C
  3. 3
    ترشيحThe product was filtered off
  4. 4
    غسيلwashed with a small amount of DCM

الإجراء التجريبي

Experimental conditions analogous to those described for Step 3 of Example 1, from 127 mg (0.46 mmol) of 3-(5,6-dimethyl-pyridine-2-carbonyl)-1H-quinolin-4-one, 22 mg (0.55 mmol) of 60% sodium hydride, 155 mg (0.55 mmol) of N-(6-bromomethyl-pyridin-2-yl)-2,2,2-trifluoro-acetamide and 1 mL of N,N-dimethylformamide. The 130 mg of trifluoroacetamide product were heated to 60° C. in a mixture of 1 mL of methanol and 4 mL of diethylamine for 3 h, then overnight at 45° C. The product was filtered off and washed with a small amount of DCM. Yield: 36 mg of a white solid: LC-MSD, m/z for C23H20N4O2 [M+H]+=385.2; HPLC retention time: 0.8 min.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07557213B2uspto-grants-2009_07