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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288684Generated: November 1, 2026

Methyl iodide → HCID 21254871, compound

https://huagongshe.com/reaction/2288684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21996863HCID 21996863—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21254871HCID 2125487147%

Reaction Steps

Under anhydrous conditions, a solution of [2-chloro-4-(1-methyl-1H-pyrazol-3-yl)-phenyl]-(5,11-dihydro-pyrido[2,3-b][1,5]benzodiazepin-10-yl)-methanone of Example 19 (0.382 g, 0.92 mmol) in 10 mL of tetrahydrofuran was added dropwise to a stirred slurry of hexane washed sodium hydride (0.025 g, 1.02 mmol) in 2 mL of tetrahydrofuran. After the gas evolution ceased, methyl iodide (1 mL) was added and stirring was continued for 2 hours. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine and dried over sodium sulfate. The solvent was removed and the crude product purified by flash chromatography (on silica Merck-60, dichloromethane-ethyl acetate 2:1) to give the title compound (0.18 g, 47%). Crystallization from diethylether provided a light yellow solid (0.16 g), m.p. 249-250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090803
Source datasetuspto-grants-2000_07
ORD IDord-1c899f0f54e041c69dbecbe248ed659c
Source noteuspto-grants-2000_07