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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016451Generated: October 29, 2026

Ammonia → 7-(2-Aminoethylamino)-2,5-dimethyl-3-(4-chloro-2,6-dimethylphenyl)-pyrazolo[1,5-a] pyrimidine

https://huagongshe.com/reaction/1016451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthylenediamineHCID 3301—
ReactantDichloromethaneHCID 6344—
Reactant7-Chloro-2,5-dimethyl-3-(4-chloro-2,6-dimethylphenyl)-pyrazolo[1,5-a]pyrimidineHCID 18406982—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product7-(2-Aminoethylamino)-2,5-dimethyl-3-(4-chloro-2,6-dimethylphenyl)-pyrazolo[1,5-a] pyrimidineHCID 18407001—

Reaction Steps

Dissolve 7-chloro-2,5-dimethyl-3-(4-chloro-2,6-dimethylphenyl)-pyrazolo[1,5-a] pyrimidine in 25 mL CH3CN, then add excess ethylenediamine (5 mL) and heat to 80° C. for 3-6 h under N2 with attached reflux condenser. (TLC; product diamine Rf=0.5, aryl chloride Rf=1.0; [10% (2.0M NH3 in MeOH)/90% CH2Cl2] as eluent). Cool to ambient temperature and evaporate to yellow oil. Partition between CH2Cl2 (50 mL) and 1.0 N NaOH (50 mL), and extract aqueous layer 2×30 mL CH2Cl2. Pool organic layers, dry over Na2SO4, filter and evaporate to yellow-white foam (1.25 g). Use without further purification. LCMS=344.4 (MH+); 342.3 (M−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476038B1
Source datasetuspto-grants-2002_11
ORD IDord-e6ff041fd1a84426be5bc129f7f7787d
Source noteuspto-grants-2002_11