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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602144Generated: October 25, 2026

3-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]methoxymethyl]piperidine → Methyl 3-[3-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]methoxymethyl]piperidin-1-yl]benzoate

https://huagongshe.com/reaction/602144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]methoxymethyl]piperidineHCID 57572215—
Reactant3-Methoxycarbonylphenylboric acidHCID 67170287—
ProductMethyl 3-[3-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]methoxymethyl]piperidin-1-yl]benzoateHCID 5899267979.4%

Reaction Steps

Using 3-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]methoxymethyl]piperidine (62.2 mg, 0.185 mmol) and 3-(methoxycarbonyl)phenylboric acid (66.6 mg, 0.370 mmol), the same procedure was followed as in Example 2 to obtain 69.2 mg (79%) of the desired compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902367B2
Source datasetuspto-grants-2011_03
ORD IDord-f0c75d01800343d398242ac8c7ec85bc
Source noteuspto-grants-2011_03