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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111343Generated: November 2, 2026

Methyl 2-methyl-3-[(phenylmethyl)amino]propanoate → HCID 87617944, compound

https://huagongshe.com/reaction/2111343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-methyl-3-[(phenylmethyl)amino]propanoateHCID 97781—
ReactantPotassium BicarbonateHCID 516893—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 87617944HCID 8761794469.9%

Reaction Steps

To a mixture of 2.73 g (0.010 mole) of (rac)-3-benzylamino-2-methyl-propanoic acid methyl ester, 1.84 g (0.010 mole) of 2,4-dichloro-5-nitro-pyrimidine, 50 mL of ethyl acetate and 25 mL of water was added 3.0 g (0.030 mole) of potassium bicarbonate. The mixture was stirred for 3 hours, then diluted with 50 mL of ethyl acetate and 50 mL of water. The layers were separated, and the aqueous layer extracted twice with 100 mL of ethyl acetate. The organic layers were washed with 100 mL of brine, combined, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with dichloromethane-ethyl acetate (100:0-97:3) to give 2.55 g of (rac)-3-[benzyl-(2-chloro-5-nitro-pyrimidin-4-yl)-amino]-2-methyl-propanoic acid methyl ester (IV-42) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517873B2
Source datasetuspto-grants-2009_04
ORD IDord-208ab84748304e679a14ab5cbfddaf05
Source noteuspto-grants-2009_04