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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71421Generated: October 23, 2026

4-Nitro-1,3-benzenediamine → N2,N4-bis(3-amino-4-nitrophenyl)-5-fluoro-2,4-pyrimidinediamine

https://huagongshe.com/en/reaction/71421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitro-1,3-benzenediamineHCID 21208—
Reactant2,4-Dichloro-5-fluoropyrimidineHCID 250705—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN2,N4-bis(3-amino-4-nitrophenyl)-5-fluoro-2,4-pyrimidinediamineHCID 22060904—

Reaction Conditions

Temperature70 °C

Reaction Steps

2,4-Dichloro-5-fluoropyrimidine (50 mg, 0.3 mmol) was dissolved in a mixture of MeOH (1 ml) and H2O (0.1 ml). 3-amino-4-nitroaniline (184 mg, 1.2 mmol) was added and the mixture was refluxed for 3 days (70° C. oil-bath temperature). The mixture was cooled to 22° C., concentrated to dryness under reduced pressure and subjected to column chromatography on silica gel (CHCl3—Acetone, 2:1) to give N2,N4-bis(3-amino-4-nitrophenyl)-5-fluoro-2,4-pyrimidinediamine. 1H NMR (DMSO-d6+CD3OD): δ 8.21 (d, 1H, J=2.9 Hz), 7.89 (m, 3H), 7.56 (d, 1H, J=2.3 Hz), 7.01 (m, 1H), 6.81 (dd, 1H, J=2.3, 9.4 Hz); LCMS: purity: 91.1%; MS (m/e): 401.00 (M+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822685B2
Source datasetuspto-grants-2014_09
ORD IDord-81c250b3c3224d4598b1e7961ad3e752
Source noteuspto-grants-2014_09