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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397963Generated: November 1, 2026

4-Aminopyridine → 3-(indolin-1-ylsulfonyl)-N-(pyridin-4-yl)benzamide

https://huagongshe.com/reaction/1397963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
Reactant3-(2,3-dihydro-1H-indole-1-sulfonyl)benzoic acidHCID 3807505—
Product3-(indolin-1-ylsulfonyl)-N-(pyridin-4-yl)benzamideHCID 24980452—

Reaction Steps

3-(indolin-1-ylsulfonyl)benzoic acid (3) (200 mg, 0.66 mmol) and 4-aminopyridine (52 mg, 0.55 mmol) using method C. The residue was purified using flash chromatography eluting with 30-90 EtOAc in hexanes. The resulting solid was triturated with dichloromethane/hexanes to give 3-(indolin-1-ylsulfonyl)-N-(pyridin-4-yl)benzamide as an off-white solid. Yield: 86 mg (43%). 1H-NMR: 10.81 (s, 1H), 8.50 (d, J=6.0 Hz, 2H), 8.35 (t, J=1.5 Hz, 1H), 8.24 (dt, J=8.0, 1.0, 1.0, 1H), 8.01 (dt, J=8.0, 1.0, 1.0, 1H), 7.77-7.72 (m, 3H), 7.50 (d, J=8.0 Hz, 1H), 7.21 (t, J=7.5 Hz, 1H), 7.16 (d, J=7.0 Hz, 1H), 6.99 (dt, J=7.5, 7.5, 1.0 Hz, 1H), 3.98 (t, J=8.5 Hz, 2H), 2.91 (t, J=8.5 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901306B2
Source datasetuspto-grants-2014_12
ORD IDord-98f94319e019426ca07e9d108df26f01
Source noteuspto-grants-2014_12