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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531276Generated: October 27, 2026

Indan-5-amine → 2-Bromo-N-indan-5-yl-5-nitro-benzamide

https://huagongshe.com/reaction/1531276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndan-5-amineHCID 90496—
Reactant4''-Trifluoromethyl-biphenyl-2-carboxylic acid (2-benzenesulfonylamino-indan-5-yl)-amideHCID 9893362—
Reactant2-Bromo-5-nitrobenzoyl chlorideHCID 11471072—
Product2-Bromo-N-indan-5-yl-5-nitro-benzamideHCID 21253366—

Reaction Steps

2-Bromo-N-indan-5-yl-5-nitro-benzamide is prepared similarly to the title E compound of Example 1 using the title A compound, 2-bromo-5-nitrobenzoyl chloride (1.07 g, 4.06 mmol) and 5-aminoindan (0.54 g, 4.06 mmol). 1H NMR (DMSO-d6, 300 MHz): δ 10.52 (1H, s), 8.34 (1H, d), 8.21 (1H, dd), 8.03 (1H, d), 7.60 (1H, s), 7.38 (1H, d), 7.19 (1H, d), 2.85 (4H, m), 2.02 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197798B1
Source datasetuspto-grants-2001_03
ORD IDord-a935927ef9414c679508a4e87a2ff010
Source noteuspto-grants-2001_03