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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986918Generated: November 1, 2026

4-[1-(3-Bromo-5-methyl-thiophen-2-yl)-1-hydroxyimino-methyl]-piperidine-1-carboxylic acid tert-butyl ester → 4-(5-Methyl-thieno[2,3-d]isoxazol-3-yl)-piperidine-1-carboxylic acid

https://huagongshe.com/reaction/1986918

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[1-(3-Bromo-5-methyl-thiophen-2-yl)-1-hydroxyimino-methyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 72434560—
CatalystCopper iodideHCID 83717—
Product4-(5-Methyl-thieno[2,3-d]isoxazol-3-yl)-piperidine-1-carboxylic acidHCID 23112436—

Reaction Steps

Prepared essentially as 2211-198 except that 4-[1-(3-bromo-5-methyl-thiophen-2-yl)-1-hydroxyimino-methyl]-piperidine-1-carboxylic acid tert-butyl ester is used as the starting material. Two other differences are: 1) 0.05 equivalents of copper iodide is used, and 2) no partition between ethyl acetate and water accompanied by subsequent extraction with ethyl acetate is required. Purification of the residue via flash column chromatography uses a mixture of ethyl acetate: n-heptane (1:4) to yield a white solid. LC/MS (ESI), m/e 345 (MNa+), retention time 2.12 minutes. Condition II.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550469B2
Source datasetuspto-grants-2009_06
ORD IDord-b835dce252d840beb1e1d31167f70c06
Source noteuspto-grants-2009_06