HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269763Generated: October 25, 2026
4-(1-Pyrrolidinyl)piperidine → Balamapimod
https://huagongshe.com/reaction/269763
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(1-Pyrrolidinyl)piperidine | HCID 78703 | — |
| Reactant | 4-[3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamino]-7-fluoro-6-methoxyquinoline-3-carbonitrile | HCID 23498074 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Balamapimod | HCID 11478684 | 71.7% |
Reaction Steps
A mixture of 150 mg (0.34 mmol) of 4-[3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)-phenylamino]-7-fluoro-6-methoxyquinoline-3-carbonitrile and 316 mg (2.05 mmol) of 4-pyrrolidin-1-yl-piperidine in 1 mL of 1-methyl-2-pyrrolidinone is heated at 105° C. for 16 hours. The solvents are removed in vacuo. A 10 mL portion of water is added to the residue, from which a tan solid is precipitated out. The solid is filtered off and washed with water. After drying in vacuo, the solid is suspended in ethyl acetate and stirred for 1 hour. The solid is filtered off, washed with ethyl acetate and dried in vacuo to provide 140 mg of 4-[3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)-phenylamino]-6-methoxy-7-(4-pyrrolidin-1-yl-piperidin-1-yl)-quinoline-3-carbonitrile as a yellow solid, mp 225-229° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449460B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-5e993a61203246509d41e42f5748b5aa |
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| Source note | uspto-grants-2008_11 |
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