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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572550Generated: October 31, 2026

Sodium Bicarbonate → Tert-butyl 2-[(3-cyano-5-fluorobenzyl)amino]-4-methylpentanoate

https://huagongshe.com/reaction/572550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-(Bromomethyl)-5-fluorobenzonitrileHCID 66652629—
Reactantethyl D-leucine tert-butyl ester hydrochlorideHCID 86683829—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-[(3-cyano-5-fluorobenzyl)amino]-4-methylpentanoateHCID 66653018—

Reaction Steps

To 3-(bromomethyl)-5-fluorobenzonitrile (4.0 g, 0.02 mol) in dry DMF (40 mL) were added sodium bicarbonate (3.9 g, 0.046 mol) and ethyl D-leucine tert-butyl ester hydrochloride (4.2 g, 0.019 mol). The reaction mixture was stirred at RT for 16 hours. It was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, brine, dried and concentrated. The crude product was purified by chromatography using petroleum ether/ethyl acetate as eluent, affording the title compound as a colorless liquid. 1H NMR (DMSO-d6, 400 MHz): δ 7.68 (d, J=9.5 Hz, 1H), 7.63 (s, 1H), 7.53 (d, J=9.8 Hz, 1H), 3.78 (d, 1H), 3.64 (d, 1H), 2.97 (d, 1H), 2.60 (brs, 1H), 1.97-1.71 (m, 1H), 1.36 (m, 11H), 0.86 (d, 3H), 0.80 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029405B2
Source datasetuspto-grants-2015_05
ORD IDord-bcce3e61c9314fc5b18183fc1762c4e5
Source noteuspto-grants-2015_05