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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366367Generated: October 30, 2026

1-Methylpiperazine → HCID 67226785, compound

https://huagongshe.com/reaction/2366367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant3,4-DimethoxybenzeneacetonitrileHCID 66727—
Reactant5-Bromothiophene-2-carbaldehydeHCID 78428—
ReactantHCID 60694908HCID 60694908—
ProductHCID 67226785HCID 6722678567%

Reaction Steps

Through the procedure as employed in Production step 1, an amine moiety derived from 1-methylpiperazine (6.01 g) was introduced into 5-bromothiophene-2-carboxaldehyde (3.82 g), to thereby yield 5-(4-methyl-piperazin-1-yl)-thiophene-2-carbaldehyde (yield: 3.71 g, 88%). The produced 5-(4-methyl-piperazin-1-yl)-thiophene-2-carbaldehyde (2.10 g) was condensed with 3,4-dimethoxybenzyl cyanide (1.77 g) through Method A (production step 2), to thereby yield the target product (yield: 2.47 g, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697742B2
Source datasetuspto-grants-2014_04
ORD IDord-b20e2908dbef4165bcc587243f552873
Source noteuspto-grants-2014_04