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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402223Generated: October 27, 2026

4-Fluoro-3-(trifluoromethyl)aniline → HCID 178505120, compound

https://huagongshe.com/reaction/2402223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-3-(trifluoromethyl)anilineHCID 75377—
ReactantN-hydroxy-4-({2-[(methylsulfonyl)amino]ethyl}amino)-1,2,5-oxadiazole-3-carboximidamideHCID 136330166—
ProductHCID 178505120HCID 178505120—

Reaction Steps

The title compound was prepared according to the procedure of Example 17 step E, using N′-hydroxy-4-({2-[(methylsulfonyl)amino]ethyl}amino)-1,2,5-oxadiazole-3-carboximidamide and 3-trifluoromethyl-4-fluoroaniline [Aldrich, product #217778] as the starting materials. LCMS for C13H15F4N6O4S (M+H)+: m/z=427.0. 1H NMR (400 MHz, DMSO-d6): δ 11.60 (s, 1H), 9.07 (s, 1H), 7.30 (t, J=10.1 Hz, 1H), 7.18 (t, J=6.0 Hz, 1H), 7.13 (dd, J=6.0, 2.7 Hz, 1H), 7.03 (m, 1H), 6.27 (t, J=6.3 Hz, 1H), 3.32 (m, 2H), 3.13 (q, J=6.0 Hz, 2H), 2.89 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796319B2
Source datasetuspto-grants-2014_08
ORD IDord-bce5ebd06a62417ab4c23c433819c71c
Source noteuspto-grants-2014_08