تفاعل #45456

معادلة التفاعل

4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridine-7-carboxylic acid

0-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate

1-hydroxybenzotriazole hydrate

diisopropylethylamine

2-[(2-aminoethyl)(2-hydroxyethyl)amino]ethanol

→

N7-2-[di(2-hydroxyethyl)amino]ethyl-4-amino-3-(3-methoxy-4-[(1-methyl-1H-2-indolyl)carbonyl]aminophenyl)thieno[3,2-c]pyridine-7-carboxamide

المذيبات

N,N-dimethylformamide

ظروف التفاعل

المعالجة

1. 1
   أخرىThe vial was flushed with nitrogen gas
2. 2
   أخرىUpon completion of the reaction, methylene chloride (2 mL) and saturated sodium bicarbonate solution (2 mL)
3. 3
   workup.ADDITIONwere added
4. 4
   ترشيحThe solution was filtered through an Empore™ cartridge
5. 5
   أخرىthe solvents removed under reduced pressure
6. 6
   غسيلeluted (gravity) through a Si-carbonate™ cartridge (2 gram, 6 mL)
7. 7
   أخرىThe organic solution obtained
8. 8
   تركيزwas concentrated
9. 9
   أخرىthe resulting residue triturated with water

الإجراء التجريبي

A 20 mL scintillation vial was charged with 4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridine-7-carboxylic acid (0.070 g, 0.148 mmol), 0-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.067 g, 0.177 mmol), 1-hydroxybenzotriazole hydrate (0.024 g, 0.177 mmol) and N,N-dimethylformamide (1.5 mL). To the suspension was added diisopropylethylamine (0.100 mL, 0.592 mmol) and 2-[(2-aminoethyl)(2-hydroxyethyl)amino]ethanol (0.024 mg, 0. 162 mmol). The vial was flushed with nitrogen gas prior to capping, and the reaction mixture was shaken at room temperature for 12 hours. Upon completion of the reaction, methylene chloride (2 mL) and saturated sodium bicarbonate solution (2 mL) were added. The solution was filtered through an Empore™ cartridge, and the solvents removed under reduced pressure. The residues were taken up in a minimal amount of methanol and eluted (gravity) through a Si-carbonate™ cartridge (2 gram, 6 mL). The organic solution obtained was concentrated and the resulting residue triturated with water to give N7-2-[di(2-hydroxyethyl)amino]ethyl-4-amino-3-(3-methoxy-4-[(1-methyl-1H-2-indolyl)carbonyl]aminophenyl)thieno[3,2-c]pyridine-7-carboxamide as a precipitate. The title compound was collected and dried by vacuum filtration (15 mg, 14%). LCMS (Conditions a) Rt 2.62 min., 603.4 (MH+); 1H NMR (400 MHz, DMSO-d6) δ 9.51 (s, 1 H), 8.51 (s, 1 H), 8.39 (t, J=5.5 Hz, 1 H), 7.99 (dd, J=7.8 Hz, 8.2 Hz, 1 H), 7.70 (d, J=8.2 Hz, 1 H), 7.59 (d, J=7.2 Hz, 1 H), 7.58 (s, 1 H), 7.35 (s, 1 H), 7.32 (d, J=8.2 Hz, 1 H), 7.20 (d, J=1.6 Hz, 1 H), 7.15 (dd, J=7.8 Hz, 7.2 Hz, 1 H), 7.07 (dd, J=8.2 Hz, 1.6 Hz, 1 H), 4.41 (t, J=5.8 Hz, 1 H), 4.04 (s, 3 H), 3.91 (s, 3 H), 3.44 (q, J=5.8 Hz, 4 H), 3.34 (m, 2 H), 2.68 (t, J=7.2 Hz, 2 H), 2.61 (t, J=5.8 Hz, 4 H).

المصدر