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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632576Generated: October 24, 2026

Sodium Bicarbonate → 1-cyclopentyl N-{3-[(methylamino)methyl]benzyl}-L-leucinate

https://huagongshe.com/en/reaction/632576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant3-(Bromomethyl)benzaldehydeHCID 7127825—
ReactantL-leucine cyclopentyl ester tosylateHCID 86633653—
SolventMethanolHCID 887—
Solvent1,1-DichloroethaneHCID 6365—
SolventEthyl AcetateHCID 8857—
Product1-cyclopentyl N-{3-[(methylamino)methyl]benzyl}-L-leucinateHCID 8668642615.2%

Reaction Steps

To a solution of 3-(bromomethyl)-benzaldehyde (0.513 g, 2.57 mmol) in dichloroethane (10 mL) was added L-leucine cyclopentyl ester tosylate (1.29 g, 3.46 mmol) and sodium triacetoxyborohydride (1.37 g, 6.46 mmol). The mixture was stirred for 30 minutes at room temperature then poured into ethyl acetate (200 mL). The organic extracts were washed with saturated ammonium chloride (2 times 50 mL) and water (50 mL). The organic extracts were then dried (MgSO4) and concentrated. The residue was dissolved in ethanol (30 mL) and methylamine hydrochloride (4.17 g, 61.7 mmol) was added followed by sodium hydrogen carbonate (4.32 g, 51 mmol). The mixture was stirred at room temperature for 18 hours then concentrated under vacuum, loaded directly onto a silica gel column and eluted with 95:5 dichloromethane:methanol to yield the desired product (0.130 g, 15% yield). LC/MS: m/z 333.25 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321718B2
Source datasetuspto-grants-2016_04
ORD IDord-91e262448bd24c2a981e1bc01796de64
Source noteuspto-grants-2016_04