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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(methylcarbamoyl)piperidine-1-carboxylateHCID 2757240—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132426B2
Source datasetuspto-grants-2006_11
ORD IDord-055f1f8443e14536b86e2acb881951b3
Source noteuspto-grants-2006_11