HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889177Generated: October 30, 2026
Potassium Carbonate → HCID 66760760, compound
https://huagongshe.com/reaction/889177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 2-bromopropanoate | HCID 545327 | — |
| Reactant | 479611-85-3 | HCID 11672769 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66760760 | HCID 66760760 | — |
Reaction Steps
To a suspension of N-methylpiperazine-1-carboxamide hydrochloride (6 g, 33.52 mmol) and K2CO3 (9.26 g, 67.0 mmol) in acetonitrile (100 mL) was added bromopropionic acid tert-butyl ester (8.4 g, 40.2 mmol). The reaction mixture was stirred at reflux for 12 h, cooled to room temperature and partitioned in ethyl acetate (200 mL) and water (100 mL). Organic layer was separated, dried (MgSO4), and concentrated to give tert-butyl 3-(4-(methylcarbamoyl)piperazin-1-yl)propanoate as an oil which was dissolved in a mixture of dichloromethane (100 mL) and TFA (trifluoroacetic acid) (20 mL) and then stirred overnight. The volatiles were removed under vacuum. The residue was dissolved in methanol, 1N hydrogen chloride in ether was added, and then the solution was concentrated to give 3-(4-(methylcarbamoyl)piperazin-1-yl)propanoic acid as a solid. LCMS 216 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252793B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-38ba2ed12d1041d6af9b6abb9c2453f6 |
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| Source note | uspto-grants-2012_08 |
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