Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-fluoro-3-(piperidin-4-yl)-1H-indole | HCID 11769929 | — |
| Reactant | HCID 69747384 | HCID 69747384 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86587529 | HCID 86587529 | — |
Reaction Steps
A solution of 4-methoxy-3-(4-methylpiperazin-1-yl)aniline dihydrochloride (2.65 g; 9 mmol), triethylamine (4.5 ml; 31.5 mmol) and N,N′-carbonyldiimidazole (1.6 g; 10 mmol) in 125 ml of acetonitrile is stirred at room temperature for 3 hours. A suspension of 2.0 g (9 mmol) of 5-fluoro-3-piperidin-4-yl-1H-indole and 1.3 ml (9 mmol) of triethylamine in 125 ml of acetonitrile is added to the mixture and it is stirred at room temperature for a further 12 hours. After customary working up, the residue is dissolved in acetone and the hydrochloride is precipitated using 1N HCl. By recrystallization from ethanol/diethyl ether, 4-(5-fluoro-1H-indole-3-yl)piperidine-1-carboxylic acid [4-methoxy-3-(4-methylpiperazin-1-yl)phenyl]amide hydrochloride is obtained
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06509340B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-05b6366d641c462495ca3144e69871b2 |
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| Source note | uspto-grants-2003_01 |
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