Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619246Generated: November 1, 2026

Acetic Acid → HCID 23728856, compound

https://huagongshe.com/reaction/1619246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 59588794HCID 59588794—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23728856HCID 2372885654.8%

Reaction Conditions

Temperature63 °C

Reaction Steps

To a solution of 2-(4-cyclopropylpiperazin-1-yl)benzothiazole-6-carboxaldehyde (500 mg, 1.7 mmol) in MeOH (14 mL) and THF (28 mL) was added piperidine (290 mg, 3.4 mmol), acetic acid (22 mg, 0.4 mmol) and NaCNBH3 (158 mg, 2.7 mmol). The mixture was stirred at 63° C. overnight. The reaction mixture was concentrated under reduced pressure and CH2Cl2 (15 mL) was added to the residue. The mixture was washed with brine, dried (MgSO4) and concentrated under reduced pressure. The residue was purified by preparative HPLC to give 332 mg (28%) of 2-(4-cyclopropylpiperazin-1-yl)-6-(piperidin-1-ylmethyl)benzothiazole as a trifluoroacetate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772285B2
Source datasetuspto-grants-2014_07
ORD IDord-21ca9527213441adaeee0fc66d3ab9ec
Source noteuspto-grants-2014_07