HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966526Generated: October 31, 2026
1-Methylpiperazine → 2-Methyl-5-[2-(4-methyl-piperazin-1-yl)-ethyl]-1H-indole-3-carboxylic Acid Benzyl Ester
https://huagongshe.com/reaction/966526
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 5-(2-Methanesulfonyloxy-ethyl)-2-methyl-1H-indole-3-carboxylic Acid Benzyl Ester | HCID 23393852 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Methyl-5-[2-(4-methyl-piperazin-1-yl)-ethyl]-1H-indole-3-carboxylic Acid Benzyl Ester | HCID 10293866 | 45% |
Reaction Steps
To a solution of 5-(2-methanesulfonyloxy-ethyl)-2-methyl-1H-indole-3-carboxylic acid benzyl ester (424 mg, 1.1 mmol, Example 56, Step D) in dioxane (10 mL) was added 1-methylpiperazine (0.6 mL, 5.5 mmol). The mixture was stirred at 70° C. overnight and then partitioned between methylene chloride and water. The organic phase was washed with water and brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo to give a solid residue, which was recrystallized from ethyl acetate to give 191 mg (45%) of the desired product as a white solid: mp 167-168° C.; MS(APCI+): m/z 392.3 (MH+); Anal. Calcd for C24H29N3O2.0.5H2O: C, 71.97; H, 7.55; N, 10.49. Found: C, 72.35; H, 7.54; N, 10.12.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06951848B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-7f54fb7d9d3a45908df322ae218cb249 |
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| Source note | uspto-grants-2005_10 |
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