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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706714Generated: October 31, 2026

Acetic Anhydride → 1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone

https://huagongshe.com/reaction/706714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant4-nitro-1-(piperidin-3-ylmethyl)-1H-indazoleHCID 67976102—
SolventDichloromethaneHCID 6344—
Product1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanoneHCID 6797459152.4%

Reaction Steps

A solution of 4-nitro-1-(piperidin-3-ylmethyl)-1H-indazole (0.050 g, 0.139 mmol), triethylamine (0.097 mL, 0.699 mmol) in DCM (1 mL) was treated with acetic anhydride (0.0158 mL, 0.168 mmol) at ambient temperature and stirring continued for 1 hour. The mixture was quenched with saturated aqueous sodium bicarbonate, extracted with DCM, dried (phase separator silicone treated filter paper) and concentrated to provide 1-(3-((4-nitro-1H-indazol-1-yl)methyl)piperidin-1-yl)ethanone (0.022 g, 52% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174981B2
Source datasetuspto-grants-2015_11
ORD IDord-4401c4df7ecc4bcdb731aef308c135d0
Source noteuspto-grants-2015_11