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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415308Generated: October 29, 2026

Ammonia → Benzyl 3-(7-carbamoylbenzo[d]oxazol-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/415308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethyl 2-(1-(benzyloxycarbonyl)piperidin-3-yl)benzo[d]oxazole-7-carboxylateHCID 66620844—
SolventMethanolHCID 887—
ProductBenzyl 3-(7-carbamoylbenzo[d]oxazol-2-yl)piperidine-1-carboxylateHCID 6662143326%

Reaction Steps

Methyl 2-(1-(benzyloxycarbonyl)piperidin-3-yl)benzo[d]oxazole-7-carboxylate (360 mg, 0.92 mmol) was added to a solution of ammonia in methanol (10 mL) and the mixture was stirred at room temperature overnight. Then the mixture was evaporated under reduced pressure and extracted with ethyl acetate (100 mL×4), the organic phase was dried with anhydrous sodium sulfate and evaporated under reduced pressure. 200 mg benzyl 3-(7-carbamoylbenzo[d]oxazol-2-yl)piperidine-1-carboxylate was obtained. Yield: 26%. LC-MS (ESI) m/z: 380 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-da0d6d833b11436f8d378319cccda2e1
Source noteuspto-grants-2012_01