Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552438Generated: November 1, 2026

3-(Trifluoromethoxy)benzoyl chloride → HCID 45140536, compound

https://huagongshe.com/reaction/552438

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethoxy)benzoyl chlorideHCID 522854—
ReactantHCID 45140146HCID 45140146—
ProductHCID 45140536HCID 4514053633%

Reaction Steps

Method H was used with 4-(3-amino-4-chlorophenoxy)-3-nitropyridin-2-amine and 3-(trifluoromethoxy)benzoyl chloride to afford the title compound as a yellow solid (0.153 g, 33%). 1H NMR δ (DMSO): 6.11 (d, 1H, Hpy,5, J=5.5 Hz), 7.18 (dd, 1H, Harom,5, J=3+9 Hz), 7.23 (s, 2H, NH2), 7.53 (d, 1H, Harom,2, J=3 Hz), 7.63 (dt, 1H, Harom, J=1+8 Hz), 7.66 (d, 1H, Harom,6, J=9 Hz), 7.70 (t, 1H, Harom,5, J=8 Hz), 7.91 (s, 1H, Harom,2′), 8.02 (dt, 1H, Harom, J=1+8 Hz), 8.07 (d, 1H, Hpy,6, J=5.5 Hz), 10.63 (s, 1H, NHamide). 19F NMR δ (DMSO): −56.37 (s, 3F, CF3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951819B2
Source datasetuspto-grants-2011_05
ORD IDord-28148f5bfb364d41b1e0fbf1a3150599
Source noteuspto-grants-2011_05