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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602145Generated: October 25, 2026

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

https://huagongshe.com/reaction/602145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]methoxy]piperidineHCID 57572149—
Reactant3-Methoxycarbonylphenylboric acidHCID 67170287—
ProductMethyl 3-[3-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]methoxy]piperidin-1-yl]benzoateHCID 5899260672%

Reaction Steps

Using 3-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]methoxy]piperidine (60.2 mg, 0.186 mmol) and 3-(methoxycarbonyl)phenylboric acid (66.9 mg, 0.372 mmol), the same procedure was followed as in Example 2 to give 61.0 mg (72%) 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-bebcab066b2e47f39b8610b154c97af9
Source noteuspto-grants-2011_03