HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716415Generated: November 3, 2026
1-Methylpiperazine → HCID 16059211, compound
https://huagongshe.com/reaction/1716415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 16059210 | HCID 16059210 | — |
| Product | HCID 16059211 | HCID 16059211 | 22% |
Reaction Steps
A mixture of 20 mg (0.041 mmol) of (1-benzyl-2-methyl-1H-indol-3-yl)-[4-(2-chloro-benzoimidazol-1-yl)-piperidin-1-yl]-methanone (the preparation of which is described in example 1) and N-methyl-piperazine was heated in a sealed tube at 90° C. for 8 hours, cooled to RT and then concentrated in vacuo. Flash chromatography (CH2Cl2/MeOH 9/1) afforded 5 mg (22%) of (1-benzyl-2-methyl-1H-indol-3-yl)-{4-[2-(4-methyl-piperazin-1-yl)-benzoimidazol-1-yl]-piperidin-1-yl}-methanone as white solid. ES-MS m/e (%): 547.5 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803815B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-ec0bc9abad99435587628696caab5aa1 |
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| Source note | uspto-grants-2010_09 |
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