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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472597Generated: October 30, 2026

tert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylate → HCID 59612611, compound

https://huagongshe.com/reaction/472597

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylateHCID 21940085—
ReactantHCID 67481566HCID 67481566—
ProductHCID 59612611HCID 59612611—

Reaction Steps

4-{4-[8-(4-Difluoromethyl-2-methoxy-phenyl)-[1,2,4]-triazolo[1,5-a]pyridin-2-ylamino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester was prepared from 2-chloro-8-(4-difluoromethyl-2-methoxy-phenyl)-[1,2,4]-triazolo[1,5-a]pyridine (0.150 g, 0.484 mmol) and 4-(4-amino-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (0.161 g, 0.581 mmol) in a manner analogous to Example 311a and 311b to give product (0.191 g, 72%). MP=95-100° C. 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 9.57 (s, 1H), 8.78 (d, 1H), 7.70 (d, 1H), 7.55 (m, 3H), 7.32 (s, 1H), 7.25 (m, 1H), 7.15 (d, 2H), 7.10 (br m, 1H), 7.05 (m, 1H), 4.10 (m, 2H), 3.78 (s, 3H), 2.78 (br m, 2H), 2.55 (m, 1H), 1.75 (m, 2H), 1.45 (m, 2H), 1.41 (s, 9H): MS=550 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633173B2
Source datasetuspto-grants-2014_01
ORD IDord-4c711d503d7d4a109d93d00b26e4720d
Source noteuspto-grants-2014_01