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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177436Generated: October 31, 2026

Avadomide → N-(3-(2,6-dioxopiperidin-3-yl)-2-methyl-4-oxo-3,4-dihydroquinazolin-5-yl)formamide

https://huagongshe.com/reaction/2177436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAvadomideHCID 24967599—
Reactant3-(2-methyl-5-nitro-4-oxo-4H-quinazolin-3-yl)-piperidine-2,6-dioneHCID 66642982—
SolventFormic AcidHCID 284—
ProductN-(3-(2,6-dioxopiperidin-3-yl)-2-methyl-4-oxo-3,4-dihydroquinazolin-5-yl)formamideHCID 90000864—

Reaction Steps

In another embodiment, provided herein is a method for preparing 3-(5-amino-2-methyl-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione, or an enantiomer or a mixture of enantiomers thereof; or a pharmaceutically acceptable salt, solvate, hydrate, or polymorph thereof; comprising the steps of (a) reducing 3-(2-methyl-5-nitro-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione in a solvent in the presence of formic acid to form N-(3-(2,6-dioxopiperidin-3-yl)-2-methyl-4-oxo-3,4-dihydroquinazolin-5-yl)formamide; and (b) hydrolyzing N-(3-(2,6-dioxopiperidin-3-yl)-2-methyl-4-oxo-3,4-dihydroquinazolin-5-yl)formamide in a solvent to form 3-(5-amino-2-methyl-4-oxoquinazolin-3(4H)-yl)piperidine-2,6-dione, or an enantiomer or a mixture of enantiomers thereof; or a pharmaceutically acceptable salt, solvate, hydrate, or polymorph thereof; wherein steps (a) and (b) are each as described herein elsewhere.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067912B2
Source datasetuspto-grants-2015_06
ORD IDord-02c8dd50d3644507aee1b1109b438580
Source noteuspto-grants-2015_06