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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599282Generated: October 30, 2026

2-Chloro-4-fluoro-5-nitroaniline → HCID 86629440, compound

https://huagongshe.com/reaction/599282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-fluoro-5-nitroanilineHCID 20234502—
ReactantHCID 86629436HCID 86629436—
SolventPyridineHCID 1049—
ProductHCID 86629440HCID 8662944056%

Reaction Conditions

Temperature50 °C

Reaction Steps

2-Chloro-4-fluoro-5-nitro-phenylamine (1.4 g, 7.4 mmol) was added to a solution of 5-(chloromethyl)-N2-methoxy-N2,N4-dimethylpyridine-2,4-diamine from example A16 (1.6 g, 7.4 mmol) in pyridine (30 mL) and the mixture was stirred at 50° C. for 8 hours. The reaction mixture was concentrated under reduced pressure and the solid residue was thoroughly washed with water to give 5-((2-chloro-4-fluoro-5-nitrophenylamino)methyl)-N2-methoxy-N2,N4-dimethylpyridine-2,4-diamine (1.5 g, 56% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.01 (s, 1H), 7.76 (d, J=8.4 Hz, 1 H), 7.71 (s, 1 H), 7.34 (d, J=8 Hz, 1 H), 6.56 (m, 1 H), 5.98 (s, 1 H), 4.36 (d, J=4 Hz, 2 H), 3.71 (s, 3 H), 3.31 (s, 3 H), 2.91-2.92 (d, J=4 Hz, 3 H); MS (ESI) m/z: 369.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897762B2
Source datasetuspto-grants-2011_03
ORD IDord-dc2dde2bdcd2470493bad7a8e9291bd4
Source noteuspto-grants-2011_03