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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133763Generated: October 25, 2026

4-Amino-2-chlorobenzonitrile → 3-(3-Chloro-4-cyanophenylamino)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide

https://huagongshe.com/reaction/133763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2-chlorobenzonitrileHCID 88728—
Reactant2-Methyl-N-(3-methyl-4-nitrophenyl)oxirane-2-carboxamideHCID 71420003—
Product3-(3-Chloro-4-cyanophenylamino)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamideHCID 67526543—

Reaction Steps

3-(3-Chloro-4-cyanophenylamino)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide was prepared as described in Example 52 starting from 4-amino-2-chlorobenzonitrile and 2-methyloxirane-2-carboxylic acid (3-methyl-4-nitrophenyl)amide. The crude product was purified by flash chromatography (dichloromethane-3% methanol). 1H NMR (400 MHz, DMSO-d6): 1.40 (3H, s), 2.52 (3H, s), 3.27 (1H, dd, J=13.8 Hz, J=5.5 Hz), 3.55 (1H, dd, J=13.8 Hz, J=6.9 Hz), 6.12 (1H, s), 6.72 (1H, dd, J=8.8 Hz, J=2.2 Hz), 6.90 (1H, d, J=2.2 Hz), 6.95-6.98 (1H, m), 7.46 (1H, d, J=8.7 Hz), 7.80 (1H, dd, J=8.9 Hz, J=2.3 Hz), 7.83 (1H, d, J=2.0 Hz), 8.02 (1H, d, J=8.9 Hz), 10.05 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390923B2
Source datasetuspto-grants-2008_06
ORD IDord-1f71bd822ec74e30993542ccd0d0ab3b
Source noteuspto-grants-2008_06