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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59979Generated: October 29, 2026

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

https://huagongshe.com/reaction/59979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-amino-4-[3-(trifluoromethyl)phenyl]piperidine-1-carboxylateHCID 43811007—
Reactant4-oxo-1H-1,2,3-benzotriazine-8-carboxamideHCID 178513613—
Product4-((4-(3-(Trifluoromethyl)phenyl)piperidin-3-yl)amino)benzo[d][1,2,3]triazine-8-carboxamideHCID 76072994—

Reaction Steps

Compound 21 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-(3-(trifluoromethyl)phenyl)piperidine-1-carboxylate to give the title compound. LC-MS [417 (M+H)], 1H NMR (400 MHz, DMSO-d6) δ 9.24 (s, 1H), 8.98 (d, 1H), 8.84 (t, 1H), 8.54 (d, 1H), 8.50 (d, 1H), 8.30 (d, 1H), 8.04-7.89 (m, 2H), 7.67 (s, 1H), 7.59 (t, 1H), 7.45 (d, 2H), 5.42-5.26 (m, 1H), 3.64 (d, 1H), 3.49 (d, 1H), 3.35 (td, 1H), 3.23-2.90 (m, 2H), 2.52-2.00 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440968B2
Source datasetuspto-grants-2016_09
ORD IDord-ad56ad7dfa584ebc9d82eeca90ce1478
Source noteuspto-grants-2016_09