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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404409Generated: October 30, 2026

4-Amino-1-methylpiperidine → HCID 86695318, compound

https://huagongshe.com/reaction/2404409

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantHCID 66836093HCID 66836093—
CatalystTitaniumHCID 23963—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodiumHCID 5360545—
ProductHCID 86695318HCID 86695318—

Reaction Steps

To a solution of (benzothiazol-2-yl)(m-tolyl)methanone (1.06 g) and 4-amino-1-methylpiperidine (0.456 g) in tetrahydrofurane (4 mL) is added titanium tetraisopropoxyde (1.42 g). The mixture is stirred at room temperature for 1 h, then polymethyl hydrosiloxane (1.2 mL) is added. The mixture is stirred for one day at room temperature, diluted with ethyl acetate (50 mL), hydrolysed with 3N sodium hydroxyde (30 mL). The organic phase is separated by decantation, washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue is cristallised by trituration in diisopropyl oxyde. A second crop can be obtained form the mother liquor by chromatography over silica gel (gradiant dichloromethane/methanol from 98/2 to 95/5) to give [(benzothiazol-2-yl)(m-tolyl)methylene](1-methylpiperidin-4-yl)amine meting at 125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802664B2
Source datasetuspto-grants-2014_08
ORD IDord-428261af7b7e45d39e1d8893c781e5ef
Source noteuspto-grants-2014_08