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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092705Generated: October 27, 2026

Sodium hydride → 4-Chloro-6-(2-ethylpiperidino)-5-fluoropyrimidine

https://huagongshe.com/reaction/1092705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-EthylpiperidineHCID 94205—
Reactant4,6-Dichloro-5-fluoropyrimidineHCID 11286675—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-6-(2-ethylpiperidino)-5-fluoropyrimidineHCID 5934111775.4%

Reaction Steps

0.07 g of sodium hydride (60% oil suspention) was suspended in 3 ml of tetrahydrofuran. 1 ml of tetrahydrofuran solution of 0.14 g of 2-ethylpiperidine was added dropwise at room temperature therein slowly, and the mixture was stirred for 10 minutes. Into the mixture was added dropwise 1 ml of tetrahydrofuran solution of 0.2 g of 4,6-dichloro-5-fluoropyrimidine at room temperature, and stirred for 4 hours. The reaction mixture was poured into a saturated ammonium chloride aqueous solution, and the mixture was extracted with tert-butyl methyl ether three times. The organic layers were washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.22 g of 4-chloro-6-(2-ethylpiperidino)-5-fluoropyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129526B2
Source datasetuspto-grants-2012_03
ORD IDord-896c4e4a048b4a15a332024a94746bb8
Source noteuspto-grants-2012_03