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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944690Generated: October 29, 2026

Acetic Acid → [2-(4-Isopropylpiperazin-1-yl)benzothiazol-5-yl-methyl]dimethylamine

https://huagongshe.com/reaction/1944690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(4-Isopropylpiperazin-1-yl)benzothiazole-5-carbaldehydeHCID 59588793—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product[2-(4-Isopropylpiperazin-1-yl)benzothiazol-5-yl-methyl]dimethylamineHCID 2372889546%

Reaction Steps

To a solution of 2-(4-isopropylpiperazin-1-yl)benzothiazole-5-carbaldehyde (500 mg, 1.73 mmol) and dimethylamine hydrochloride (282 mg, 3.46 mmol) in THF (27.5 mL) and MeOH (13.7 mL) was added acetic acid (166 mg, 2.77 mmol), followed by NaCNBH3 (160 mg, 2.77 mmol). The mixture was heated at reflux overnight. The mixture was concentrated under reduced pressure, neutralized with an aqueous solution of Na2CO3 to pH 7, and filtered. The residue was extracted with dichloromethane (3×10 mL). The combined organic extracts were washed with brine, dried (Na2SO4) and concentrated. The residue was purified by preparative HPLC to give 251 mg (46%) of [2-(4-isopropylpiperazin-1-yl)benzothiazol-5-yl-methyl]dimethylamine as a trifluoroacetate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394842B2
Source datasetuspto-grants-2013_03
ORD IDord-14e310191fc54dc695b3f6f65b401a9c
Source noteuspto-grants-2013_03