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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039533Generated: October 31, 2026

5-(3-Nitro-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamine → 5-(3-Amino-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamine

https://huagongshe.com/reaction/2039533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(3-Nitro-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamineHCID 67042802—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
Product5-(3-Amino-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamineHCID 6992755268.9%

Reaction Steps

To a solution of 5-(3-nitro-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamine (0.10 g, 0.31 mmol), prepared as described in Example 2, in N,N-dimethylformamide (10 mL), 10% Pd/C (50% w/w, 0.05 g) was added. The mixture was reacted in Parr Apparatus at 40 p.s.i. for 5 h. The suspension was filtered through Celite®. After washing the filter with methanol, the solution was evaporated to dryness. The crude was twice crystallized from ethyl acetate to provide the title product (0.062 g, 67% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580783B2
Source datasetuspto-grants-2013_11
ORD IDord-749b572815d34ab989a5d2dd2c7e4ac1
Source noteuspto-grants-2013_11