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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890437Generated: October 31, 2026

7-Methoxy-1,2-dihydroquinoxalin-2-one → 3-(7-methoxy-2-oxo-2H-quinoxalin-1-ylmethyl)-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1890437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Methoxy-1,2-dihydroquinoxalin-2-oneHCID 491319—
ReactantTert-butyl 3-((methanesulfonyloxy)methyl)azetidine-1-carboxylateHCID 21959416—
Product3-(7-methoxy-2-oxo-2H-quinoxalin-1-ylmethyl)-azetidine-1-carboxylic acid tert-butyl esterHCID 6713086735.7%

Reaction Steps

Using the procedure of Example 2, step 2.i, but starting from 7-methoxy-2(1H)-quinoxalinone (1.00 g; prepared according to WO 2006/134378) and 3-[[(methylsulfonyl)oxy]methyl]-1-azetidinecarboxylic acid tert-butyl ester (1.65 g; prepared according to WO 02/066470), the second eluting compound was isolated as a yellow oil (700 mg, 35% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507478B2
Source datasetuspto-grants-2013_08
ORD IDord-a36b14d8feac4a84bbd60456c9333f2d
Source noteuspto-grants-2013_08