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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503274Generated: October 30, 2026

Sodium hydride → HCID 70937836, compound

https://huagongshe.com/reaction/1503274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 70925639HCID 70925639—
ReactantHCID 86673011HCID 86673011—
SolventDimethylformamideHCID 6228—
ProductHCID 70937836HCID 7093783680%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (RS)-benzyl 1,5,5-trimethyl-2-oxopyrrolidine-3-carboxylate (206 mg, 787 μmol) in 4 ml of dry DMF was purged with argon and cooled to 0° C. Then a 60% suspension of sodium hydride (31.5 mg, 0.79 mmol) was added and the mixture was stirred for 40 min at room temperature whereby a white suspension was formed. Then 2-chloro-5-(phenylethynyl)pyrimidine (CAS: [1051388-40-9]) (130 mg, 606 μmol) was added, the mixture was stirred for 30 min at 80° C., and then quenched by addition of 1 ml of saturated ammonium chloride solution. After extraction with ethyl acetate/water, drying over sodium sulfate and concentration; the residue (440 mg, yellow oil) was taken up in ethyl acetate, adsorbed onto 3 g of silicagel and loaded onto a 20 g prepacked flash chromatography column. After elution with a 10% to 60% ethyl acetate in heptane gradient, the fractions containing the desired product were collected to yield 212 mg (80%) of the title compound as a light yellow waxy solid, MS: m/e=440.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212171B2
Source datasetuspto-grants-2015_12
ORD IDord-248f95eace144b31bbda1f98a06a5975
Source noteuspto-grants-2015_12