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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662952Generated: October 29, 2026

Water → 1-[4-(2-(Azepan-1-yl)ethoxy)benzyl]-5-(benzyloxy)-2-(4-(benzyloxy)phenyl)-3-methyl-1H-indole

https://huagongshe.com/reaction/1662952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1H-Indole, 3-methyl-5-(phenylmethoxy)-2-[4-(phenylmethoxy)phenyl]-HCID 3824745—
Reactant1-(2-(4-(Chloromethyl)phenoxy)ethyl)azepaneHCID 9882910—
SolventDimethylformamideHCID 6228—
Product1-[4-(2-(Azepan-1-yl)ethoxy)benzyl]-5-(benzyloxy)-2-(4-(benzyloxy)phenyl)-3-methyl-1H-indoleHCID 9895831—

Reaction Steps

In an inert atmosphere NaH (2.7 g; 112 mmol) was suspended in DMF (80 ml). At 0-5° C. 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole (11 g; 26 mmol) was added and the suspension was stirred for 30 minutes. Then a solution of 4-(2-azepan-1-yl-ethoxy)benzyl chloride (8 g; 26 mmol) in DMF (30 ml) was added dropwise within 1 hour. The cooling was shut down and the reaction mixture was stirred for another 2.5 hours. Then, water (1.2 ml) was carefully added dropwise to the reaction mixture and the reaction mixture was filtered through a thin layer of celite. Another 35 ml of water were added dropwise to the brightly yellow filtrate under intensive stirring.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034807B2
Source datasetuspto-grants-2011_10
ORD IDord-1167146e9d4a4807badd7e70125e4c4c
Source noteuspto-grants-2011_10