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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986207Generated: October 30, 2026

1-(3-Aminopropyl)-4-methylpiperazine → 2-{5-Methyl-2-[3-(4-methylpiperazin-1-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-6-sulfonic acid benzhydryl-amide

https://huagongshe.com/reaction/1986207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(2-Chloro-5-methylpyrimidin-4-yl)-benzo[b]thiophene-6-sulfonic acid benzhydrylamideHCID 86625355—
Solvent1,4-DioxaneHCID 31275—
Product2-{5-Methyl-2-[3-(4-methylpiperazin-1-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-6-sulfonic acid benzhydryl-amideHCID 68855935—

Reaction Conditions

Temperature97 °C

Reaction Steps

To a stirred suspension of 2-(2-chloro-5-methylpyrimidin-4-yl)-benzo[b]thiophene-6-sulfonic acid benzhydrylamide (457 mg, 0.903 mmol) in dry 1,4-dioxane (4.5 mL) is added diisopropylethylamine (0.315 mL, 1.81 mmol) and 1-(3-aminopropyl)-4-methylpiperazine (213 mg, 1.35 mmol). The mixture is heated at 97° C. for 1 day. After concentration and subsequent chromatographic purification on silica gel, eluting with 2 M NH3/MeOH in dichloromethane: 0-10%, the title compound is obtained as a yellow solid (317 mg, 57% yield). ES+(m/z) 627 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-4a2623fd4c16422d8fc7962b616cf0d3
Source noteuspto-grants-2009_06