HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978280Generated: October 29, 2026
1-Methylpiperazine → N-[2-(5-bromo-1-indolinyl)phenyl]-4-methyl-1-piperazinecarboxamide
https://huagongshe.com/reaction/978280
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | N-[2-(5-bromo-1-indolinyl)phenyl]phenylcarbamate | HCID 131715128 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[2-(5-bromo-1-indolinyl)phenyl]-4-methyl-1-piperazinecarboxamide | HCID 13823366 | 90% |
Reaction Steps
A solution of N-[2-(5-bromo-1-indolinyl)phenyl]phenylcarbamate (11.5 g, 28.5 mmoles), N-methylpiperazine (15 ml) and ether (50 ml) was stirred at room temperature for 2 hours. The ether was evaporated. The mixture was filtered through a silica gel column (150 g), packed with dichloromethaane, and the column was washed with 2% methanol-dichloromethane solution (2 l). The solvent was evaporated. The residue was purified by flash chromatography on a silica gel column (150 g, 230-400 mesh), eluted with 1% methanol/dichloromethane (4 l), 1.5% methanol/dichloromethane (2 l), and 2% methanol/dichloromethane. The fractions containing the desired material were collected and evaporated to give 10.9 g (90%) of product. Crystallization from chloroform and hexane afforded the analytical sample, mp 108°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663453 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-8e7e68cf282544d0aed3861d68c9b481 |
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| Source note | uspto-grants-1987_05 |
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