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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676825Generated: November 1, 2026

Sodium Bicarbonate → 3-[(2-Chloro-5-nitro-pyrimidin-4-yl)-(4-methoxy-benzyl)-amino]-2,2-difluoro-propionic acid ethyl ester

https://huagongshe.com/reaction/1676825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
Reactant3-(4-Methoxybenzylamino)-2,2-difluoropropionic acid ethyl esterHCID 58014995—
SolventEthyl AcetateHCID 8857—
Product3-[(2-Chloro-5-nitro-pyrimidin-4-yl)-(4-methoxy-benzyl)-amino]-2,2-difluoro-propionic acid ethyl esterHCID 86637521100.2%

Reaction Steps

A solution of 1.2 g (0.0044 mole) of 2,2-difluoro-3-(4-methoxy-benzylamino)-propionic acid ethyl ester) in 4 mL of ethyl acetate was added over 5 minutes to a cooled (0 degrees) mixture of 0.85 g (0.0044 mole) of 2,4-dichloro-5-nitro-pyrimidine, 1.5 g (0.018 mole) of sodium bicarbonate and 10 mL of ethyl acetate. The cooling bath was removed and the mixture stirred for 17 hours at room temperature. Activated charcoal was added and after stirring briefly, the mixture was filtered through a pad of Celite, washing the filter pad with ethyl acetate. The filtrate was concentrated under reduced pressure to give 1.9 g of 3-[(2-chloro-5-nitro-pyrimidin-4-yl)-(4-methoxy-benzyl)-amino]-2,2-difluoro-propionic acid ethyl ester (IV-291) as a yellow thick oil. This material was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003785B2
Source datasetuspto-grants-2011_08
ORD IDord-cc03866605484ff0a3ca5f75d53b55df
Source noteuspto-grants-2011_08