HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333194Generated: October 26, 2026
Hydrochloric Acid → 3(3-Methoxyphenyl)-N,N,2-trimethyl pentane-1-amine hydrochloride, (2R,3R)-
https://huagongshe.com/reaction/333194
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3(3-Methoxyphenyl)-N,N,2-trimethyl pentane-1-amine, (2R,3R)- | HCID 11253328 | — |
| Reactant | (2R,3S)-3-(3-methoxyphenyl)-N,N,2-trimethylpentan-1-amine | HCID 11299316 | — |
| Reactant | Talabostat mesylate | HCID 11522448 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3(3-Methoxyphenyl)-N,N,2-trimethyl pentane-1-amine hydrochloride, (2R,3R)- | HCID 24786081 | 63% |
Reaction Steps
A mixture of (2R,3R)-3-(3-methoxyphenyl)-N,N,2-trimethylpentan-1-amine and (2R,3S)-3-(3-methoxyphenyl)-N,N,2-trimethylpentan-1-amine (10 kg, 42.56 mol, ratio 5.5:1) was dissolved in acetone (50 L) in a 100 L double jacket vessel equipped with an electrical impeller stirrer, a gas transition line, Pt100 temperature measuring equipment and an oil based cooling/heating system. Hydrogen chloride (1.55 kg, 42.51 mol) was transferred within 15 minutes at a temperature of 5° C. to 25° C. through the reaction mixture. The reaction mixture was cooled to 0° C. to 5° C. and centrifuged after 2 hours of stirring. The humid solid was put into a stirring vessel, acetone (30 L) was added and the reaction mixture was heated to reflux for 15 minutes. After cooling to 15° C. to 20° C. the product was centrifuged and stored at 40° C. to 50° C. and 150 mbar for 14 hours in a drying oven. (2R,3R)-3-(3-Methoxyphenyl)-N,N,2-trimethylpentan-1-amine hydrochloride (7.17 kg, 63%) was obtained as a colorless solid with a diastereomeric excess of 100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877974B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3884e3bbd6ea45388aef05d9f5e665ba |
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| Source note | uspto-grants-2014_11 |
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