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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532674Generated: November 1, 2026

Sodium hydride → HCID 86699246, compound

https://huagongshe.com/reaction/532674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantHCID 71815237HCID 71815237—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86699246HCID 8669924672%

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C., NaH (60 percent, 0.15 g, 3.0 mmol) was added to a THF solution (15 mL) containing 5-[6-(4-Methoxy-phenyl)-4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-2-yl]-pyridin-2-ylamine (3.1 g, 2.0 mmol). Then SEM-Cl (90% pure, 0.42 mL, 2 mmol) was added to the reaction mixture and the resulting mixture was stirred at 0° C. for 30 min, warmed up to 80° C. and stirred for 2 hr. The solution was cooled to room temperature and poured into ice water. The resulting mixture was extracted with ethyl acetate. The organic layer was collected and washed with saturated aqueous NH4Cl, dried over MgSO4(s), and concentrated under reduced pressure. The oily residue was purified by gravity column chromatography (20% EtOAc in hexane) to give 5-[6-(4-Methoxy-phenyl)-4-(2-trimethylsilanyl-ethoxymethyl)-4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-2-yl]-pyridin-2-ylamine (0.7 g, 1.44 mmol) as brown solid in 72% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853207B2
Source datasetuspto-grants-2014_10
ORD IDord-5bd1c9f380f6408895762dccd4374b74
Source noteuspto-grants-2014_10