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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227696Generated: October 26, 2026

N-(1-acetyl-5-nitro-1H-indazol-3-yl)acetamide → N-(1-acetyl-5-amino-1H-indazol-3-yl)acetamide

https://huagongshe.com/reaction/227696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-acetyl-5-nitro-1H-indazol-3-yl)acetamideHCID 57755833—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-(1-acetyl-5-amino-1H-indazol-3-yl)acetamideHCID 5775586698%

Reaction Steps

The product from Step (b) above (3.0 g, 11.4 mmol) and 5% Pd/C (1 g) were combined in MeOH (40 mL) and hydrogenated uner a balloon of H2 for 3 h. The mixture was filtered through Celite and the filtrate was concentrated to give the title compound as a dark solid (2.6 g, 98%). NMR 1H NMR (400 MHz, DMSO-D6) δ 10.62 (s, 1H), 7.97 (dd, J=7.9, 1.8, 1H), 6.93-6.89 (m, 2H), 5.26 (s, 2H), 2.52 (s, 3H), 2.08 (s, 3H) (MS m/z 233.2 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560467B2
Source datasetuspto-grants-2009_07
ORD IDord-3fa5aba120e84866967b923e5c38957f
Source noteuspto-grants-2009_07