تفاعل #2293550

ord-5056897b72c64d4a9ceef64e273bbd5f

معادلة التفاعل

O=P(O)(O)O
H3PO4
O=P(O)(O)O
H3PO4
COc1ccc(CN(c2cccc(C(=O)NCCN(C)C)c2)c2cc(Cl)nn3c(C#N)cnc23)cc1
253D
COc1ccc(CN(c2cccc(C(=O)NCCN(C)C)c2)c2cc(Cl)nn3c(C#N)cnc23)cc1
3-((6-Chloro-3-cyanoimidazo[1,2-b]pyridazin-8-yl)(4-methoxybenzyl)amino)-N-(2-(dimethylamino)ethyl)benzamide
CC(=O)Nc1cc(N)ccc1C
N-(5-amino-2-methylphenyl) acetamide
CC(=O)Nc1cc(Nc2cc(Nc3cccc(C(=O)NCCN(C)C)c3)c3ncc(C#N)n3n2)ccc1C
3-(6-(3-Acetamido-4-methylphenylamino)-3-cyanoimidazo[1,2-b]pyridazin-8-ylamino)-N-(2-(dimethylamino)ethyl)benzamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىB=100, gradient time 4 min.
  2. 2
    أخرىhold at 100% 1 min., flow rate 4 mL/min.

الإجراء التجريبي

Example 253 was prepared from 253D and N-(5-amino-2-methylphenyl) acetamide following the procedure as described in Example 6. HPLC: Rt=3.110 min. (YMC S5 ODS (4.6×50 mm) 0%-100% B. Solvent B: (90% MeOH, 10% H2O, 0.2% H3PO4). Solvent A: (10% MeOH, 90% H2O, 0.2% H3PO4). Gradient, start % B=0, final % B=100, gradient time 4 min., hold at 100% 1 min., flow rate 4 mL/min.). MS (ES): m/z=512.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ ppm 10.04 (1 H, br. s.), 9.52-9.58 (2 H, m), 9.21 (1 H, s), 8.94 (1 H, t, J=5.52 Hz), 8.18 (1 H, s), 7.87 (1 H, s), 7.59-7.63 (2 H, m), 7.44-7.54 (2 H, m), 7.06 (1 H, d, J=8.28 Hz), 6.81-6.85 (1 H, m), 3.59 (3 H, q, J=5.69 Hz), 3.24 (2 H, q, J=5.86 Hz), 2.73-2.84 (6 H, m), 2.08 (3 H, s), 1.98 (3 H, s).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09371328B2uspto-grants-2016_06