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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265220Generated: October 30, 2026

p-Nitrophenylacetonitrile → 4-Chloro-2-(2,6-difluoro-benzenesulfonylamino)-N-[2-(4-nitro-phenyl)-propyl]-benzamide

https://huagongshe.com/reaction/2265220

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-NitrophenylacetonitrileHCID 68386—
Reactantbeta-Methyl-p-nitrophenethylamine hydrochlorideHCID 3029819—
Reactant2-(2,6-Difluoro-benzenesulfonylamino)-4-chloro-benzoic acidHCID 68770444—
Product4-Chloro-2-(2,6-difluoro-benzenesulfonylamino)-N-[2-(4-nitro-phenyl)-propyl]-benzamideHCID 11699127—

Reaction Steps

This compound was prepared from 4-chloro-2-(2,6-difluoro-benzenesulfonylamino)-benzoic acid and 2-(4-nitro-phenyl)-propylamine hydrochloride (prepared as in EXAMPLE 5, substituting 4-nitrophenylacetonitrile in Part A) as in Example 1, Part C. HPLC: RT=10.37 min. MS (ESI−): mass calcd. for C22H18ClF2N3O5S, 509.9; m/z found, 509 [M−H]−. 1H NMR (400 MHz, CDCl3): 11.63 (s, 1H), 8.18 (d, J=8.6, 1H), 7.69 (d, J=1.7, 1H), 7.56-7.46 (m, 1H), 7.42 (d, J=8.6, 2H), 7.15 (d, J=8.5, 1H), 7.02-6.94 (m, 1H), 6.19-6.17 (br m, 1H), 3.79-3.70 (m, 1H), 3.57-3.49 (m, 1H), 3.33-3.23 (m, 1H), 1.38 (d, J=6.9, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855292B2
Source datasetuspto-grants-2010_12
ORD IDord-e902e91f09194918aef66e222ad0b0a4
Source noteuspto-grants-2010_12