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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162057Generated: October 29, 2026

2-Methylpiperazine → 3-Methyl-1-[(5-nitro-1-benzofuran-7-yl)methyl]piperazine

https://huagongshe.com/reaction/1162057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpiperazineHCID 66057—
Reactant7-(Bromomethyl)-5-nitrobenzofuranHCID 53402971—
Product3-Methyl-1-[(5-nitro-1-benzofuran-7-yl)methyl]piperazineHCID 6689321095%

Reaction Steps

The title compound was prepared according to the procedure of Example 112, Step 1, starting from 7-(bromomethyl)-5-nitro-1-benzofuran (120 mg, 70 mol %, 0.39 mmol; Intermediate 64) and 2-methylpiperazine (196 mg, 1.95 mmol). The crude product was purified by flash chromatography (eluent: 4% MeOH, 1% NEt3 in DCM). The title compound (102 mg, 87%) was obtained as a light yellow sticky oil. HPLC 99%, RT=1.60 min (System A; 5-60% MeCN over 3 min), 100%, RT=1.40 min (System B; 5-60% MeCN over 3 min). MS (ESI+) for C14H17N3O3 m/z 276 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820675B2
Source datasetuspto-grants-2010_10
ORD IDord-94bfdf0ab8264c828fd51f5012a15411
Source noteuspto-grants-2010_10