Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892408Generated: October 28, 2026

O-ethylhydroxylamine hydrochloride → (E)-N-ethoxy-1-[3-(1-quinolin-6-ylcyclopropyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]ethanimine

https://huagongshe.com/reaction/1892408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ethylhydroxylamine hydrochlorideHCID 76850—
Reactant1-(3-(1-(Quinolin-6-yl)cyclopropyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanoneHCID 58190510—
SolventDichloromethaneHCID 6344—
Product(E)-N-ethoxy-1-[3-(1-quinolin-6-ylcyclopropyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]ethanimineHCID 50991538—

Reaction Steps

A solution of 1-(3-(1-(quinolin-6-yl)cyclopropyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanone (30 mg, 0.09 mmol) and O-ethyl-hydroxylamine hydrochloride (18 mg, 0.18 mmol) in 2 mL of DCM was stirred at 40° C. overnight. The solvent was removed under reduced pressure and the residue was purified by flash chromatography on silica gel eluting with EtOAc/methanol gradient to afford the title compound. 1H-NMR (400 MHz, CDCl3) 3 ppm 8.84 (d, 1H), 8.29 (d, 1H), 8.25 (d, 1H), 7.92-7.91 (m, 2H), 7.72-7.68 (m, 2H), 7.49 (dd, 1H), 4.26 (q, 2H), 2.01 (s, 3H), 1.76 (s, 2H), 1.66 (s, 2H), 1.27 (t, 3H). LCMS (method A): [MH]+=373, tR=5.56 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507676B2
Source datasetuspto-grants-2013_08
ORD IDord-30cec5a60cdd4a12b0e021566808d770
Source noteuspto-grants-2013_08