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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354022Generated: October 31, 2026

Methyl iodide → HCID 10271777, compound

https://huagongshe.com/reaction/1354022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10270942HCID 10270942—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 10271777HCID 1027177761.3%

Reaction Steps

Sodium hydride (60% suspension, 0.10 g, 2.5 mmol) washed with hexane and dried under nitrogen, was suspended in dry N,N-dimethylformamide (15 mL). Following addition of 1,1′-biphenyl-4-yl-(5,11-dihydro-benzo[b]pyrido[2,3-e][1,4]diazepin-6-yl)-methanone of Example 4 (0.76 g, 2.0 mmol), methyl iodide (0.15 mL, 2.4 mmol) was added. After stirring for 1 hour, the reaction was quenched with water and extracted with dichloromethane The organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give a yellow solid. Purification of the residue by flash chromatography using a solvent gradient from 25% to 35% of ethyl acetate in hexane gave a white foam which was redissolved in dichloromethane, concentrated in vacuo to a foam, then crystallized by sonication from ethyl acetate/hexane to provide the title compound (0.48 g, 61.3%) as a white solid, m.p. 220–223° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223752B2
Source datasetuspto-grants-2007_05
ORD IDord-a19c9a5302234c7c9df09f9ef46a48d7
Source noteuspto-grants-2007_05