Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230699Generated: October 30, 2026

Sodium hydride → HCID 18464522, compound

https://huagongshe.com/reaction/2230699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl(2-iodoethoxy)dimethylsilaneHCID 11129873—
Reactant1-t-butoxycarbonyl-4-(1H-benzimidazol-2-yl)[1,4]diazepaneHCID 18464655—
ReactantDichloromethane ethylacetateHCID 21226138—
SolventDimethylformamideHCID 6228—
ProductHCID 18464522HCID 18464522—

Reaction Conditions

Temperature80 °C

Reaction Steps

Alternately, combine 1-(t-butoxycarbonyl)-4-(1H-benzimidazol-2-yl)[1,4]diazepane (1.72 g, 5.43 mmol) and sodium hydride (0.36 g, 60% in oil, 8.15 mmol) in dimethylformamide (40 mL). After 4 hours, add 2-(t-butyldimethylsilyloxy)ethyl iodide (1.56 g, 5.43 mmol). After 72 hours, heat to 80° C. After 3 hours, cool to ambient temperature and add ice to quench. Partition the reaction mixture between ethyl acetate (250 mL) and a saturated aqueous solution of sodium bicarbonate (200 mL). Separate the layers and extract the organic layer with water. Dry the organic layer over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 40% ethyl acetate/dichloromethane to give 1-(t-butoxycarbonyl)-4-(1-(2-(t-butyldimethylsilyloxy)ethyl)-1H-benzimidazol-2-yl)[1,4]diazepane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-0cc9941b78264c74bc572d0cbf45b3d4
Source noteuspto-grants-2002_07