Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870954Generated: November 4, 2026

Sodium hydride → HCID 86695946, compound

https://huagongshe.com/reaction/870954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
ReactantHCID 86695947HCID 86695947—
SolventDimethylformamideHCID 6228—
ProductHCID 86695946HCID 8669594646.2%

Reaction Steps

To a stirred solution of N-(8-chloro-5-methyl-5H-chromeno[3,4-c]pyridin-2-yl)acetamide (250 mg, 0.866 mmol) in DMF (25 mL) was added NaH (62.3 mg, 2.60 mmol) at room temperature and stirred for 10 min. 4-Methoxybenzyl chloride (0.236 mL, 1.732 mmol) was added dropwise and stirred at room temperature overnight. The reaction was quenched with ice and extracted with ethyl acetate (25 mL). The organic layer was separated, washed with water (25 mL), brine (25 mL), dried over sodium sulphate and concentrated under reduced pressure to afford 8-chloro-N,N-bis(4-methoxybenzyl)-5-methyl-5H-chromeno[3,4-c]pyridin-2-amine (200 mg, 0.20 mmol, 24% yield) as a yellow oil. This was taken to the next step without purification. LCMS (ESI) m/e 487.2 [(M+H)+, calcd for C29H28ClN2O3 487.2]; LC/MS retention time (Method C): tR=2.52 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969564B2
Source datasetuspto-grants-2015_03
ORD IDord-14df9926701d493e8a31224be15c9899
Source noteuspto-grants-2015_03