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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707516Generated: October 29, 2026

Sodium Bicarbonate → Tert-Butyl(2R)-4-(1-(diphenylmethyl)azetidin-3-yl)-2-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/707516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl (2R)-2-methylpiperazine-1-carboxylateHCID 10262201—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTert-Butyl(2R)-4-(1-(diphenylmethyl)azetidin-3-yl)-2-methylpiperazine-1-carboxylateHCID 11816247290%

Reaction Steps

To a mixed solution of a commercially available product of 1-(diphenylmethyl)azetidin-3-one (300 mg, 1.26 mmol), THF (6.0 mL) and acetic acid (500 μL) was added a commercially available product of tert-butyl(2R)-2-methylpiperazine-1-carboxylate (304 mg, 1.51 mmol) at room temperature. The resultant mixture was stirred at room temperature for 25 minutes. Sodium triacetoxyborohydride (536 mg, 2.52 mmol) was added to the reaction mixture at room temperature, and the resultant mixture was stirred at room temperature for 18 hours and 35 minutes. Sodium hydrogen carbonate and water were added to the reaction mixture, and the resultant solution was extracted with ethyl acetate. An organic layer was washed with saturated brine, then dried over anhydrous magnesium sulfate and then filtrated. The resultant residue was purified by NH silica gel column chromatography (heptane:ethyl acetate=5:1) to give the title compound (476 mg, yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174998B2
Source datasetuspto-grants-2015_11
ORD IDord-4783592622404968b19a086d0c6658eb
Source noteuspto-grants-2015_11