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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779105Generated: November 3, 2026

Diethyl Ether → tert-Butyl 4-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1779105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 2782774—
Reactanttert-butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylateHCID 27281520—
CatalystZincchlorideHCID 3007855—
Solvent1,2-DichloroethaneHCID 11—
Solventtert-ButanolHCID 6386—
Producttert-Butyl 4-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)piperidine-1-carboxylateHCID 8671228171%

Reaction Steps

A 1.0 M solution of ZnCl2 in diethyl ether (20.7 mL, 20.7 mmol) was added to a solution of 2,4-dichloro-5-(trifluoromethyl)pyrimidine (4.48 g, 20.7 mmol) in t-BuOH (100 mL) and DCE (100 mL). The mixture was stirred for 10 minutes then diluted with t-BuOH (100 mL) and DCE (100 mL) before tert-butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylate (5.00 g, 18.8 mmol) and Et3N (10.4 mL) were added. The mixture was stirred at room temperature overnight, the volatiles were removed in vacuo and the resultant residue was suspended in water (500 mL) and sonicated for 15 minutes. The solid was isolated by vacuum filtration and the filter cake washed with water (100 mL) and acetone (25 mL) to give the title compound (A133) as a tan solid (5.92 g, 71%); LCMS-A: rt 6.895 min; m/z 445.1 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266864B2
Source datasetuspto-grants-2016_02
ORD IDord-5f8ab7776bd341a9932aef13c0e269cc
Source noteuspto-grants-2016_02