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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792629Generated: November 4, 2026

[3-(Trifluoromethyl)-1-trityl-1H-pyrazol-4-YL]boronic acid → 1-[6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl)quinolin-4-yl]-piperidine-4-carboxylic acid (4-fluorophenyl)methylamide

https://huagongshe.com/reaction/1792629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-(Trifluoromethyl)-1-trityl-1H-pyrazol-4-YL]boronic acidHCID 22032227—
Reactant1-(6-Bromoquinolin-4-yl)piperidine-4-carboxylic acid (4-fluorophenyl)methylamideHCID 86760173—
Product1-[6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl)quinolin-4-yl]-piperidine-4-carboxylic acid (4-fluorophenyl)methylamideHCID 8676017290.3%

Reaction Steps

92 mg 1-(6-bromoquinolin-4-yl)piperidine-4-carboxylic acid (4-fluorophenyl)methylamide (compound in Production Example 458) and 114 mg 3-trifluoromethyl-1-trityl-1H-4-pyrazolylboronic acid (compound in Production Example 31) were reacted in the same manner as in Example 9, to give 139 mg 1-[6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl)quinolin-4-yl]-piperidine-4-carboxylic acid (4-fluorophenyl)methylamide. This product was reacted in the same manner as in Example 67, to give 80 mg of the title compound as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074801B1
Source datasetuspto-grants-2006_07
ORD IDord-4c33bc0b97a8476287958cb5a2f4d6df
Source noteuspto-grants-2006_07