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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81786Generated: October 30, 2026

5-(5-Amino-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine → 5-(2-Isopropyl-4-methoxy-5-[1,2,3]triazol-1-yl-phenoxy)-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/81786

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(5-Amino-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamineHCID 59598573—
ReactantHCID 86652241HCID 86652241—
SolventMethanolHCID 887—
Product5-(2-Isopropyl-4-methoxy-5-[1,2,3]triazol-1-yl-phenoxy)-pyrimidine-2,4-diamineHCID 5959860131%

Reaction Conditions

Temperature50 °C

Reaction Steps

Following the procedure of Harada et al., Heterocycles 1998, 48, 695-702, to a solution of 5-(5-amino-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine (0.400 g, 1.8 mmol) in 5 ml methanol at 0° C. was added trimethylamime (0.308 g, 3.0 mmol) and hydrazine 1,1-dichloroethyl hydrazine tosylate (0.388 g, 1.4 mmol). The solution was warmed to 50° C. After 4 h the mixture was concentrated in vacuo and extracted with CH2Cl2. The combined organics were washed with H2O, washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. Purification via flash chromatography (94:6 CH2Cl2/MeOH) afforded 5-(2-isopropyl-4-methoxy-5-[1,2,3]triazol-1-yl-phenoxy)-pyrimidine-2,4-diamine (0.145 g, 31%) as a white solid; [MH]+=342.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846705B2
Source datasetuspto-grants-2014_09
ORD IDord-3f4dcbed7ea346d3b3d901a8a6ad0084
Source noteuspto-grants-2014_09