HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239789Generated: November 2, 2026
Dichloromethane → 1-((3-Methylbenzo[b]thiophen-2-yl)methyl)piperazine dihydrochloride
https://huagongshe.com/reaction/2239789
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | t-Butyl 4-((3-methylbenzo[b]thiophen-2-yl)methyl)piperazine-1-carboxylate | HCID 68415560 | — |
| Product | 1-((3-Methylbenzo[b]thiophen-2-yl)methyl)piperazine dihydrochloride | HCID 68413724 | — |
Reaction Steps
The title A compound, t-butyl 4-((3-methylbenzo[b]thiophen-2-yl)methyl)piperazine-1-carboxylate is dissolved in dry DCM (50 mL), and 5 equiv. of TFA are added at 0° C. The reaction mixture is stirred at RT for 3 h. After the solvent is evaporated in vacuo, the residue is trituated in Et2O, and the precipitate that forms is collected by filtration, washed with EtOH and dried in a vacuum oven at 40° C. overnight to give a hygroscopic solid. The solid is treated with sodium bicarbonate solution, and extracted with EtOAc. The organic layer is evaporated in vacuo, and the residue is dissolved in Et2O and treated with a solution of hydrochloric acid in Et2O. The precipitated solid is collected by filtration and dried to give 1-((3-methylbenzo [b]thiophen-2-yl)methyl)piperazine dihydrochloride: LC/MS (M+1=247.1). 1H NMR (DMSO-d6, 200 MHz) δ 2.48 (s, 3H), 3.39 (m, 4H), 3.54 (m, 4H), 4.63 (s, 2H), 7.45 (m, 2H), 7.84 (d, 1H, J=7.2 Hz), 7.95 (d, 1H, J=7.2 Hz), 9.52 (br s, NH). Anal. calculated for (C14H18N2S 2HCl): C, 52.66; H, 6.31; Cl, 22.21; N, 8.77; S, 10.04. Found: C, 52.70; H, 6.58; N, 8.77; S, 9.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723343B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-56442da7b6d64b9487ef3bbbff457b4e |
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| Source note | uspto-grants-2010_05 |
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