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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482841Generated: October 30, 2026

3-Aminobenzonitrile → HCID 66761752, compound

https://huagongshe.com/reaction/1482841

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminobenzonitrileHCID 16702—
Reactant4-(1,2,3,4-Tetrahydroquinoline-1-sulfonyl)benzoic acidHCID 2318939—
ProductHCID 66761752HCID 66761752—

Reaction Steps

4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzoic acid (1) (100 mg, 0.32 mmol) was treated with 3-aminobenzonitrile (29 mg, 0.24 mmol) using method B. The residue was purified using flash chromatography eluting with 0-30% EtOAc in hexanes. The resulting solid was triturated with dichloromethane/hexanes to give N-(3-cyanophenyl)-4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzamide as a white solid. Yield: 12 mg (12%). 1H-NMR: 10.76 (s, 1H), 8.23-8.20 (m, 1H), 8.07 (d, J=8.5 Hz, 2H), 8.03-7.98 (m, 1H), 7.77 (d, J=8.5 Hz, 2H), 7.63 (d, J=8.5 Hz, 1H), 7.61-7.58 (m, 2H), 7.23-7.18 (m, 1H), 7.11-7.07 (m, 2H), 3.85-3.80 (m, 2H), 2.45 (t, J=7.0 Hz, 2H), 1.68-1.59 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416101B2
Source datasetuspto-grants-2016_08
ORD IDord-8881ce5675104b30a87493ae6e4bc773
Source noteuspto-grants-2016_08