Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157768Generated: October 30, 2026

O-Methylhydroxylamine hydrochloride → HCID 49770162, compound

https://huagongshe.com/reaction/1157768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 49770160HCID 49770160—
SolventEthanolHCID 702—
ProductHCID 49770162HCID 49770162—

Reaction Steps

To a suspension of 1-(7-acetyl-4-fluoro-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-(4-(1-phenyl-1H-tetrazol-5-yl)piperazin-1-yl)ethane-1,2-dione (0.05 g, 0.11 mmol) in EtOH (10 mL) was added methoxylamine hydrochloride (0.05 g, 0.60 mmol). The mixture was heated to reflux for 1 h, and was then cooled to rt, and concentrated in vacuo. The residue was diluted with MeOH, and the solids that formed were collected and washed with water. The title compound was isolated as a light-yellow solid (0.025 g). LCMS: m/e 492.4 (M+H)+, ret time 2.068 min (method 2). 1H NMR (500 MHz, DMSO-D6) δ ppm 12.02 (s, 1H) 8.36 (d, J=2.14 Hz, 1H) 8.27 (d, J=3.36 Hz, 1H) 7.56-7.71 (m, 5H) 4.13-4.16 (m, 3H) 3.68-3.73 (m, 2H) 3.43-3.48 (m, 2H) 3.29-3.36 (m, 2H) 3.13-3.18 (m, 2H) 2.36 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807676B2
Source datasetuspto-grants-2010_10
ORD IDord-8a1c866121e14dc389e32fb35b6c6b95
Source noteuspto-grants-2010_10