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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59980Generated: October 29, 2026

Tert-butyl 3-amino-4-[4-(trifluoromethyl)phenyl]piperidine-1-carboxylate → 4-((4-(4-(Trifluoromethyl)phenyl)piperidin-3-yl)amino)benzo[d][1,2,3]triazine-8-carboxamide

https://huagongshe.com/reaction/59980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-amino-4-[4-(trifluoromethyl)phenyl]piperidine-1-carboxylateHCID 43811008—
Reactant4-oxo-1H-1,2,3-benzotriazine-8-carboxamideHCID 178513613—
Product4-((4-(4-(Trifluoromethyl)phenyl)piperidin-3-yl)amino)benzo[d][1,2,3]triazine-8-carboxamideHCID 76073025—

Reaction Steps

Compound 22 was prepared following general synthesis scheme 9 wherein 4-hydroxybenzo[d][1,2,3]triazine-8-carboxylic acid amide was reacted with tert-butyl 3-amino-4-(4-(trifluoromethyl)phenyl)piperidine-1-carboxylate to give the title compound. LC-MS [417 (M+H)], 1H NMR (400 MHz, DMSO-d6) δ 9.21 (s, 1H), 9.04-8.92 (m, 1H), 8.61-8.43 (m, 3H), 8.11-7.92 (m, 2H), 7.72 (d, 1H), 7.64-7.46 (m, 5H), 5.58-5.44 (m, 1H), 3.71-3.44 (m, 4H), 3.30-3.09 (m, 1H), 2.81-2.60 (m, 1H), 2.08 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440968B2
Source datasetuspto-grants-2016_09
ORD IDord-1400d646d2014b6c9ea36337c4b32059
Source noteuspto-grants-2016_09