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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111417Generated: November 2, 2026

Potassium Bicarbonate → HCID 87618346, compound

https://huagongshe.com/reaction/2111417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BicarbonateHCID 516893—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
ReactantMethyl 2-methyl-3-(2-propen-1-ylamino)propanoateHCID 43398422—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 87618346HCID 8761834681%

Reaction Steps

To a mixture of 1.71 g (0.010 mole) of (rac)-2-methyl-3-(2-propenylamino)-propanoic acid methyl ester, 1.94 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, and then diluted with 50 mL of ethyl acetate and 50 mL of water. The aqueous layer was extracted 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 (100:0-97.5:2.5) to give 2.55 g of (rac)-3-[allyl-(2-chloro-5-nitro-pyrimidin-4-yl)-amino]-2-methyl-propanoic acid methyl ester (IV-65) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517873B2
Source datasetuspto-grants-2009_04
ORD IDord-97a7cd7b1ccb4c58b2162e3b59a59c24
Source noteuspto-grants-2009_04