HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418603Generated: October 26, 2026
Diisopropylethylamine → HCID 58790187, compound
https://huagongshe.com/reaction/418603
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl malonyl chloride | HCID 123460 | — |
| Reactant | tert-Butyl 4-aminopiperidine-1-carboxylate--hydrogen chloride (1/1) | HCID 2756033 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58790187 | HCID 58790187 | 78% |
Reaction Steps
The mixture of tert-butyl 4-aminopiperidine-1-carboxylate hydrochloride (512 mg, 2.16 mmol), methyl 3-chloro-3-oxopropanoate (232 μL, 2.16 mmol), and DIPEA (828 μL, 4.75 mmol) in DCM (20 mL) was stirred at room temperature overnight. The solvent was removed under reduced pressure and the residue was purified by flash chromatography (eluent EtOAc) to afford tert-butyl 4-(3-methoxy-3-oxopropanamido)piperidine-1-carboxylate as a white solid (500 mg, 78%). MS (m/z): 301.1 (M+H). This material (500 mg, 1.67 mmol) was dissolved in MeOH/THF/H2O (2 mL/2 mL/1 mL), and LiOH×H2O (280 mg, 6.75 mmol) was added to the solution. The reaction mixture was stirred for 2 hrs, the solvent was removed under reduced pressure and the residue was purified by flash chromatography (eluent CH3Cl/MeOH/AcOH) to afford the title compound 42 (300 mg, 63% yield) as yellowish syrup. MS (m/z): 287.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093264B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-939bd7dd38a748d29ac311cc2cd567a2 |
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| Source note | uspto-grants-2012_01 |
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