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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43537Generated: October 25, 2026

Sodium Bicarbonate → tert-Butyl trans(+/-)-4-amino-3-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylate

https://huagongshe.com/reaction/43537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl trans(+/-)-4-azido-3-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylateHCID 86648551—
CatalystNickel chloride dihydrateHCID 10942802—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl trans(+/-)-4-amino-3-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylateHCID 86648550—

Reaction Steps

tert-Butyl trans(±)-4-azido-3-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylate obtained in Example (79b) (265.6 mg, 0.71 mmol) was dissolved in THF (6 mL) and methanol (3 mL). Nickel chloride dihydrate (345 mg, 1.42 mmol) and sodium borohydride (117 mg, 2.85 mmol) were added under ice-cooling, and the mixture was heated to room temperature and stirred for 30 minutes. Saturated aqueous sodium bicarbonate solution was added to the reaction solution, followed by filtration through celite and extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-adeb2c8e3074407dac0647c43e8dbcda
Source noteuspto-grants-2013_09