HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719489Generated: October 30, 2026
Methylamine → Tert-butyl 4-(methylcarbamoyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/719489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid | HCID 392871 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(methylcarbamoyl)piperidine-1-carboxylate | HCID 2757240 | — |
Reaction Steps
To a stirred solution of 1-t-butoxycarbonyl-iso-nipecotic acid (10 g) and Et3N (5.92 mL) in THF (32 mL) was added drop-wise iso-butylchloroformate (5.66 mL) at 0° C. The resulting mixture was stirred at 0° C. for 30 min before diluted with THF (120 mL) and added 2M methylamine (80 mL). The reaction mixture was stirred overnight at room temperature. Excess THF was removed under vacuum. The residue was taken into H2O and extracted into EtOAc. The organic extracts were washed with 1N NaOH, followed by brine. After dried over Na2SO4, it was concentrated to give the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132426B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-055f1f8443e14536b86e2acb881951b3 |
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| Source note | uspto-grants-2006_11 |
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