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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907175Generated: October 30, 2026

Methyl iodide → HCID 59425714, compound

https://huagongshe.com/reaction/907175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 59425535HCID 59425535—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59425714HCID 5942571476%

Reaction Steps

1-Ethyl-6-methoxy-2-(3-oxo-3,4-dihydro-2H-benzo [1,4]oxazin-6-yl)-1H-indole-3-carbonitrile (20 mg, 0.058 mmol), prepared as in example 1BH, was combined with NaH (14 mg, 60% suspension in oil, 0.35 mmol). THF (300 μL) was added. This was stirred at room temperature for 5 minutes. A solution of methyl iodide (4.4 μL) in THF (100 μL) was added. This was stirred at room temperature for 1 hour. The reaction mixture was partitioned between EtOAc and aqueous HCl. The organic layer was dried and concentrated. Purification by silica gel chromatography (9/1, CH2Cl2/EtOAc) yielded 1-ethyl-6-methoxy-2-(4-methyl-3-oxo-3,4,-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-indole-3-carbonitrile (16 mg, 76%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013006B2
Source datasetuspto-grants-2011_09
ORD IDord-afa4ff74366f41928d46bb9e147d1f3a
Source noteuspto-grants-2011_09