Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36053Generated: October 26, 2026

Sodium hydride → HCID 178444711, compound

https://huagongshe.com/reaction/36053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-hexyl-3-bromomethyl-4-methoxy-6-methyl-2(1H)-quinolinoneHCID 15233349—
ReactantHCID 178418441HCID 178418441—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178444711HCID 17844471152.2%

Reaction Steps

A solution of tetrazole (0.17 g) in dimethylformamide (2 ml) at ice-bath temperature under nitrogen was stirred with 60% sodium hydride (0.1 g) for 5 mins and then a solution of 1-hexyl-3-bromomethyl-4-methoxy-6-methyl-2(1H)-quinolinone (Example 14, 0.73 g) in dimethylformamide (8 ml) was added to it. The reaction mixture was stirred at room temperature for 2 hours, diluted with ethylacetate and then washed several times with water. The organic layer was dried and evaporated under reduced pressure. The resulting crude reaction product was chromatographed on silica-gel (30 g). Elution with 10% to 20% ethylacetatedichloromethane gave 1-hexyl-3-(1-tetrazolylmethyl)-4-methoxy-6-methyl-2(1H)-quinolinone (0.37 g). That this compound was obtained was confirmed by the spectral data: MS: m/e 355 (M+); NMR (CDCl3): δ4.18 (s, 3H, OCH3), 5.68 (s, 2H, CH2), 9,14 (s, 1H, CH= ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05412104
Source datasetuspto-grants-1995_05
ORD IDord-9b2ca84c31a3491a8e38aaf5939f1239
Source noteuspto-grants-1995_05