Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491636Generated: October 27, 2026

1,2-Dichloroethane → HCID 178474213, compound

https://huagongshe.com/reaction/491636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantN-[3-(3,4-Diamino-phenoxy)-phenyl]-acetamideHCID 17755037—
Reactant1-(2-Chloro-5-isothiocyanato-benzyl)-4-methyl-piperazineHCID 17755843—
SolventAcetonitrileHCID 6342—
ProductHCID 178474213HCID 178474213—

Reaction Steps

A solution of N-[3-(3,4-diamino-phenoxy)-phenyl]-acetamide (Step B, 320 mg, 1.2 mmol, 1.0 eq.) in 20 mL of anhydrous CH3CN was added drop-wise to a solution of 1-(2-chloro-5-isothiocyanato-benzyl)-4-methyl-piperazine (300 mg, 1.2 mmol, 1.0 eq.) in 10 mL of CH3CN. The reaction was stirred for 2 h at RT. EDC (360 mg, 1.9 mmol, 1.5 eq.) was added and the reaction was heated to 80° C. and stirred for 1 h. The mixture was cooled and concentrated. The residue was dissolved into EtOAc and washed with H2O and sat. NaHCO3 (aq.). The organic layer was dried (MgSO4), filtered and concentrated. The crude was further purified by column chromatography (0-10% MeOH/CH2Cl2 with 1% NH4OH) followed by recrystallization from CH2Cl2 to give pure N-(3-{2-[4-chloro-3-(4-methyl-piperazin-1-ylmethyl)-phenylamino]-1H-benzimidazol-5-yloxy}-phenyl)-acetamide. MS m/z=506.2 (M+H)+; Calc'd for C27H29N6O2: 504.20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531553B2
Source datasetuspto-grants-2009_05
ORD IDord-9e06ca3c534041ac84d337b13dcab6f7
Source noteuspto-grants-2009_05