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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716712Generated: October 31, 2026

Triethylamine → tert-Butyl 4-[2-(tetrahydro-2H-pyran-4-yl)-1,3-oxazol-4-yl]piperidine-1-carboxylate

https://huagongshe.com/reaction/716712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantOxane-4-carboxamideHCID 13197203—
Reactanttert-Butyl 4-(2-Bromoacetyl)piperidine-1-carboxylateHCID 18187487—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Producttert-Butyl 4-[2-(tetrahydro-2H-pyran-4-yl)-1,3-oxazol-4-yl]piperidine-1-carboxylateHCID 70171103—

Reaction Steps

tert-Butyl 4-(bromoacetyl)piperidine-1-carboxylate (1.07 g, 3.49 mmol) and tetrahydro-2H-pyran-4-carboxamide (0.95 g, 7.36 mmol) were mixed heated in DMPU (6.99 mL) at 150° C. for 4 hrs. LC-MS indicated that the reaction was completed and the product showed loss of Boc group. Et3N (1.46 mL, 10.5 mol) and Boc2O (0.915 g, 4.19 mmol) were added and the mixture was stirred at RT for 30 min. The reaction was diluted with water and dichloromethane. The two layers were separated and the organic layer was extracted with dichloromethane. The combined organic layers were washed with H2O (twice) and brine, dried over Na2SO4, filtered and conc. The crude (still containing DMPU) was used without purification. LC-MS: [M+H]+=337.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193697B2
Source datasetuspto-grants-2015_11
ORD IDord-59ee269021374425940789826f7f61ca
Source noteuspto-grants-2015_11