Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | N-(4-aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide | HCID 21927707 | — |
| Reactant | 1-Acetyl-3-(1-ethoxy-1-phenylmethylene)-6-methoxycarbonyl-2-indolinone | HCID 66685972 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178497199 | HCID 178497199 | — |
Reaction Steps
10.5 g (30.0 mmol) of 1-acetyl-3-(1-ethoxy-1-phenylmethylene)-6-methoxycarbonyl-2-indolinone (for preparation see WO 01/27081 mentioned above) and 8.60 g (33.0 mmol) N-[(4-methyl-piperazin-1-yl)-methylcarbonyl]-N-methyl-p-phenylenediamine (for preparation see WO 01/27081 mentioned above) are dissolved in 80 mL of dimethylformamide and stirred for 1 hour at 80° C. After cooling 6.50 mL of piperidine are added and the mixture is stirred for another two hours at ambient temperature. Water is added, the precipitate formed is suction filtered and washed with a little water. The residue is suspended in 200 mL of methanol, suction filtered and washed with cold water and diethyl ether. The substance is dried in vacuo at 110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119093B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-01fa38e889264465aaccd3dcbf91a959 |
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| Source note | uspto-grants-2006_10 |
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