Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425092Generated: November 2, 2026

Sodium Bicarbonate → Ethyl cis(+/-)-2-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-5-methyl-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/1425092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantButyl 3-bromo-2-oxobutanoateHCID 87440690—
Reactantcis(+/-)-Benzyl (1-carbamoyl-3-methoxypiperidin-4-yl)carbamateHCID 131730860—
SolventTetrahydrofuranHCID 8028—
ProductEthyl cis(+/-)-2-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-5-methyl-1,3-oxazole-4-carboxylateHCID 13173086178.2%

Reaction Steps

The same operation as in Example (103c) was performed using cis(±)-benzyl (1-carbamoyl-3-methoxypiperidin-4-yl)carbamate obtained in Example (103b) (1.97 g, 6.4 mmol), butyl 3-bromo-2-oxobutanoate obtained in Example (106a) (10 g, 42.3 mmol), sodium bicarbonate (1.26 g, 15 mmol) and THF (40 mL). The resulting residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=1/10, 1/2, 1/1, 2/1, 4/1) to obtain 2.09 g of the title compound as a yellow oily substance (73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-3d1178fa451643feb57a13f2a8585e34
Source noteuspto-grants-2015_01