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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890033Generated: November 1, 2026

tert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylate → HCID 49839608, compound

https://huagongshe.com/reaction/1890033

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylateHCID 21940085—
Reactant2,2'-Bis(dicyclohexylphosphino)-1,1'-biphenylHCID 24946987—
Reactant[1-(4-Methylphenyl)-1H-pyrazol-4-yl]boronic acidHCID 46738688—
ReactantHCID 67481369HCID 67481369—
Reactant8-Bromo-2-chloro-[1,2,4]triazolo[1,5-a]pyridineHCID 67481370—
ProductHCID 49839608HCID 49839608—
ProductHCID 67481369HCID 67481369—

Reaction Steps

2-Chloro-8-(1-p-tolyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyridine was prepared from 8-bromo-2-chloro-[1,2,4]triazolo[1,5-a]pyridine and 1-p-tolyl-pyrazole-4-boronic acid in a manner analogous to Example 2c (0.40 g, 68%). 287b) 4-{4-[8-(1-p-Tolyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyridine-2-ylamino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester was prepared from 2-chloro-8-(1-p-tolyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyridine and 4-(4-amino-phenyl)-piperidine-1-carboxylic acid tert-butyl ester with 2,2′-bis-dicyclohexylphosphanyl-biphenyl as the ligand in a manner analogous to Example 2d (0.265 g, 40%). MP=124-125° C. 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 9.60 (s, 1H), 9.24 (s, 1H), 8.68 (d, 1H), 8.64 (s, 1H), 7.98 (m, 1H), 7.77 (m, 2H), 7.66 (m, 2H), 7.40 (m, 2H), 7.21 (m, 2H), 4.08 (m, 2H), 2.80 (m, 2H), 2.62 (m, 1H), 2.38 (s, 3H), 1.73 (m, 2H), 1.48 (m, 2H), 1.41 (s, 3H). MS=550 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501936B2
Source datasetuspto-grants-2013_08
ORD IDord-eda7a88f44dd4603ac332f0987d823b1
Source noteuspto-grants-2013_08