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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592491Generated: October 25, 2026

Diethyl Ether → Tert-butyl 1-(4-(4-chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)ethylcarbamate

https://huagongshe.com/reaction/592491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 2782774—
Reactanttert-butyl N-[1-(4-aminophenyl)ethyl]carbamateHCID 22569414—
CatalystZincchlorideHCID 3007855—
Solvent1,2-DichloroethaneHCID 11—
Solventtert-ButanolHCID 6386—
ProductTert-butyl 1-(4-(4-chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)ethylcarbamateHCID 76611269—

Reaction Steps

2,4-Dichloro-5-(trifluoromethyl)pyrimidine (1.93 g, 8.89 mmol) was stirred in a 1:1 t-BuOH:DCE mixture (200 mL) at room temperature. A 1.0 M ZnCl2 solution in Et2O (10.2 mL, 10.2 mmol) was added cautiously and the mixture was stirred at room temperature for 20 minutes. A 1:1 t-BuOH:DCE mixture (100 mL) was added followed by tert-butyl (1-(4-aminophenyl)ethyl)carbamate (2.00 g, 8.46 mmol) and Et3N (1.42 mL, 10.2 mmol). The mixture was stirred at room temperature overnight before the volatiles were evaporated in vacuo. EtOH (30 mL) was added, the suspension was sonicated for 1 minute before the solid was filtered, washed with EtOH (10 mL) and dried in vacuo to give the title compound A80 as a cream solid (3.2 g, 91%). LCMS-C: rt 4.88 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238644B2
Source datasetuspto-grants-2016_01
ORD IDord-d8c8a23f7c554cd097d6fd06c5592ac3
Source noteuspto-grants-2016_01