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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(3-Aminopropyl)-4-methylpiperazine | HCID 78328 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(2-Chloro-5-methylpyrimidin-4-yl)-benzo[b]thiophene-6-sulfonic acid benzhydrylamide | HCID 86625355 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-{5-Methyl-2-[3-(4-methylpiperazin-1-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-6-sulfonic acid benzhydryl-amide | HCID 68855935 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07547691B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-4a2623fd4c16422d8fc7962b616cf0d3 |
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| Source note | uspto-grants-2009_06 |
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