HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095533Generated: November 1, 2026
1-Methylpiperazine → HCID 15557283, compound
https://huagongshe.com/reaction/1095533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 3-(2-Bromoethyl)indole | HCID 76924 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 15557283 | HCID 15557283 | — |
Reaction Steps
3-(2-Bromo-ethyl)-indole (3.00 g, 13.39 mmol) was initially introduced into abs. CHCl3 (25 ml), and 1-methylpiperazine (2.68 g, 26.8 mmol) was added. The mixture was stirred at a bath temperature of 75° C. for 5 h and at RT overnight. The mixture was extracted dilute sulfuric acid (2×30 ml), the acidic aqueous phase was rendered alkaline with 5N NaOH, while cooling with ice, and the mixture was extracted with ether (3×30 ml). The organic phase was dried over Na2SO4 and concentrated i. vac. Yield: 1.45 g (Ind-68, 45%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138187B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-c96199b1726b47caa481c6063d9e117e |
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| Source note | uspto-grants-2012_03 |
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