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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953776Generated: November 1, 2026

5-[Di-(tert-butoxycarbonyl)amino]methyl-7-nitro-2,3-dimethoxyquinoxaline → 5-Aminomethyl-2,3-dimethoxy-7-nitro-quinoxaline

https://huagongshe.com/reaction/1953776

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-[Di-(tert-butoxycarbonyl)amino]methyl-7-nitro-2,3-dimethoxyquinoxalineHCID 23298008—
SolventTrifluoroacetic acidHCID 6422—
Product5-Aminomethyl-2,3-dimethoxy-7-nitro-quinoxalineHCID 17915296—

Reaction Steps

13.8 9 (29.7 mmol) of 5-[di-(tert-butoxycarbonyl)amino]methyl-7-nitro-2,3-dimethoxyquinoxaline are stirred at room temperature for 8 hours in 60 ml of trifluoroacetic acid. The reaction mixture is concentrated under reduced pressure and the red oil is well stirred at 0° for one hour with 1N potassium carbonate. The yellow crystals are filtered off, washed with 100 ml of water and 100 ml of a 1:1 mixture of ethyl acetate and hexane, and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117873
Source datasetuspto-grants-2000_09
ORD IDord-ceeffaaf095041cd815115f76703a569
Source noteuspto-grants-2000_09