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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990796Generated: October 25, 2026

Acetic Acid → Benzothiazol-2-yl-[1-(2-ethoxy-naphthalen-1-ylmethyl)-piperidin-4-yl]-amine

https://huagongshe.com/reaction/1990796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Ethoxynaphthalene-1-carbaldehydeHCID 88099—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-(Piperidin-4-yl)-1,3-benzothiazol-2-amineHCID 14575274—
SolventEthanolHCID 702—
ProductBenzothiazol-2-yl-[1-(2-ethoxy-naphthalen-1-ylmethyl)-piperidin-4-yl]-amineHCID 866076258%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of benzothiazol-2-yl-piperidin-4-yl-amine (23.3 mg, 0.1 mmol, 1.0 equiv) and 2-ethoxy-naphthalene-1-carbaldehyde (commercially available, 24.0 mg, 0.12 mmol, 1.2 equiv) in ethanol (2 mL) was added diisopropylethylamine (23.42 μL, 25.9 mg, 0.2 mmol, 2.0 equiv) and acetic acid (18.0 mg, 0.3 mmol, 3.0 equiv) and the mixture stirred at 40° C. After 1 h, sodium cyano borohydride (7.54 mg, 0.12 mmol, 1.2 equiv) was added and the mixture stirred at 40° C. over night. Removal of the solvent under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 3.3 mg (8%) of the title compound. MS (ESI): 418.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645753B2
Source datasetuspto-grants-2010_01
ORD IDord-8ee5054967184bad9481d5be680ac808
Source noteuspto-grants-2010_01