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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726100Generated: November 3, 2026

Triethylamine → 3-[5-(2-morpholin-4-ylethoxy)-1H-indol-2-yl]-1H-indazol-5-ol

https://huagongshe.com/reaction/1726100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium formateHCID 2723923—
ReactantHCID 136055970HCID 136055970—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-[5-(2-morpholin-4-ylethoxy)-1H-indol-2-yl]-1H-indazol-5-olHCID 13605600861.7%

Reaction Conditions

Temperature67 °C

Reaction Steps

1.12 g of 5-benzyloxy-3-[5-(2-morpholin-4-ylethoxy)-1H-indol-2-yI]-1H-indazole are dissolved in 55 ml of absolute ethanol and then 424 mg of palladium-on-charcoal, 587 mg of ammonium formate and 227 μl of triethylamine are successively added. The reaction medium is stirred at 67° C. (internal temperature of the suspension). A substantial amount of gas is seen to be given off. After stirring for one hour, the medium is filtered through paper and the catalyst is rinsed with absolute ethanol. The filtrate is concentrated under vacuum to obtain 558 mg of 3-[5-(2-morpholin-4-ylethoxy)-1H-indol-2-yl]-1H-indazol-5-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-21225314d1ea48419cfaa57a6d2bfa49
Source noteuspto-grants-2009_02