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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848739Generated: October 29, 2026

4-(Trifluoromethoxy)benzylamine → HCID 90411136, compound

https://huagongshe.com/reaction/1848739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethoxy)benzylamineHCID 571846—
ReactantHCID 12851675HCID 12851675—
Reactant3-((3-Fluoro-4-nitrophenoxy)methyl)-1-methyl-1H-pyrazoleHCID 82881970—
ReactantHCID 90411017HCID 90411017—
ProductHCID 90411136HCID 90411136—

Reaction Steps

The title compound was prepared using analogous conditions described for Example 1 using (4-(trifluoromethoxy)phenyl)methanamine and 3-((3-fluoro-4-nitrophenoxy)methyl)-1-methyl-1H-pyrazole in Step A then for Intermediate I using 5-((1-methyl-1H-pyrazol-3-yl)methoxy)-N1-(4-(trifluoromethoxy)benzyl)benzene-1,2-diamine and cis-6,6-dimethyl-3-oxabicyclo[3.1.0]hexane-2,4-dione followed by the hydrolysis according to Example 111. MS (ESI): mass calcd. for C26H25F3N4O4, 514.18; m/z found, 515.1 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 7.60 (d, J=8.9, 1H), 7.33 (d, J=2.2, 1H), 7.21 (d, J=8.1, 2H), 7.09 (d, J=8.8, 2H), 7.06 (dd, J=8.9, 2.3, 1H), 6.94 (d, J=2.2, 1H), 6.31 (d, J=2.2, 1H), 5.39 (d, J=16.9, 1H), 5.31 (d, J=16.9, 1H), 5.09 (s, 2H), 3.86 (s, 3H), 2.31 (d, J=8.2, 1H), 2.04 (d, J=8.3, 1H), 1.20 (s, 3H), 0.97 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952177B2
Source datasetuspto-grants-2015_02
ORD IDord-6729a1be20424da3abbcd7add337f618
Source noteuspto-grants-2015_02