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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531278Generated: October 31, 2026

N-(indan-5-yl)-5-nitro-2-thiophen-2-yl-benzamide → 5-amino-N-(indan-5-yl)-2-(thiophen-2-yl)-benzamide

https://huagongshe.com/reaction/1531278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(indan-5-yl)-5-nitro-2-thiophen-2-yl-benzamideHCID 21253368—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5-amino-N-(indan-5-yl)-2-(thiophen-2-yl)-benzamideHCID 21253372—

Reaction Steps

A solution of the compound of Example 5, N-(indan-5-yl)-5-nitro-2-thiophen-2-yl-benzamide (0.083 g, 0.228 mmol) in ethyl acetate (10 mL) is degassed and 10% palladium on carbon added. The reaction mixture is evacuated and placed under 1 atm H2(g) for 16 h. Filtration of the reaction mixture through Celite is followed by concentration of the filtrate under reduced pressure to give 5-amino-N-(indan-5-yl)-2-(thiophen-2-yl)-benzamide as an oil which foams to a solid on treatment with diethyl ether. mp 62-67° C. MS (ES+), m/z 335 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197798B1
Source datasetuspto-grants-2001_03
ORD IDord-ed11454e6d654e559277da24938dd3fb
Source noteuspto-grants-2001_03