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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853252Generated: November 1, 2026

O-tert-butylhydroxylamine hydrochloride → HCID 86673023, compound

https://huagongshe.com/reaction/1853252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-tert-butylhydroxylamine hydrochlorideHCID 2777906—
ReactantHCID 67194821HCID 67194821—
SolventMethanolHCID 887—
ProductHCID 86673023HCID 8667302391.4%
ProductHCID 86673025HCID 86673025—

Reaction Steps

7-bromo-2-isoquinolin-3-yl-6-methyl-chromen-4-one O-tert-butyl oxime was prepared using the method D (step 1) illustrated in example 1B. 7-bromo-2-isoquinolin-3-yl-6-methyl-chromen-4-one (730 mg, 1.98 mmol) was treated with O-tert-butyl-hydroxylamine hydrochloride (500 mg, 3.98 mmol) in methanol (13 ml) under microwave irradiation to yield 7-bromo-2-isoquinolin-3-yl-chromen-4-one O-tert-butyl oxime (383 mg, 44%) as a yellow solid after purification by flash chromatography over silica gel (cyclohexane/Chloroform/ethyl acetate: 96/4/0; 50/50/0; 0/100/0 0/50/50).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962627B2
Source datasetuspto-grants-2015_02
ORD IDord-b7a4af8804a04b07a5d8721aa46795ad
Source noteuspto-grants-2015_02