Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064306Generated: October 30, 2026

2-(3-Chloroanilino)-4-(1-triphenylmethylimidazol-4-yl)pyrimidine → 2-(3-Chloroanilino)-4-(imidazol-5-yl)pyrimidine

https://huagongshe.com/reaction/1064306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Chloroanilino)-4-(1-triphenylmethylimidazol-4-yl)pyrimidineHCID 22273504—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product2-(3-Chloroanilino)-4-(imidazol-5-yl)pyrimidineHCID 2227347475.1%

Reaction Steps

A mixture of 2-(3-chloroanilino)-4-(1-triphenylmethylimidazol-4-yl)pyrimidine (Method 2; 256 mg, 0.5 mmol) in MeOH (3 ml) and 2M hydrochloric acid (1 ml) was stirred for 15 minutes. The volatiles were removed by evaporation and the residue partitioned between EtOAc and saturated aqueous sodium hydrogen carbonate solution. The organic layer was separated, dried and the solvent removed by evaporation. The residue was purified by column chromatography eluting with DCM and 7M methanolic ammonia solution (99.5:0.5 increasing in polarity to 93:7) to give the title compound 102 mg, (75%) as a solid. NMR: 6.95 (dd, 1H), 7.25-7.33 (m, 2H), 7.73 (dd, 1H), 7.81 (d, 2H), 8.06 (s, 1H), 8.46 (d, 1H), 9.68 (s, 1H), 12.48 (br s, 1H); m/z: 270.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969714B2
Source datasetuspto-grants-2005_11
ORD IDord-c4eda35d17aa414391e683ecee4a8562
Source noteuspto-grants-2005_11