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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948447Generated: October 30, 2026

3-Hydroxypiperidine → HCID 86623159, compound

https://huagongshe.com/reaction/1948447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxypiperidineHCID 23293—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-[2-(Acetylamino)-4-methyl-1,3-thiazol-5-yl]-5-bromothiophene-2-sulfonylchlorideHCID 86623146—
SolventDichloromethaneHCID 6344—
ProductHCID 86623159HCID 86623159—

Reaction Steps

4-[2-(Acetylamino)-4-methyl-1,3-thiazol-5-yl]-5-bromothiophene-2-sulfonylchloride, prepared as in Step III of Example 23 (136 mg; 0.33 mmol; 1 eq), is dissolved in DCM (10 ml). 3-hydroxy piperidine (0.20 ml; 1.65 mmol; 5 eq) and DIEA (0.17 ml; 0.98 mmol; 3 eq) are added under a nitrogen atmosphere. After 2 hours reaction, solvents are evaporated. The crude product is dissolved in DCM and washed with NH4Cl saturated solution, water and dried over MgSO4. After evaporation of the solvents, crude material is purified by reverse preparative HPLC, affording N-(5-{2-bromo-5-[(3-hydroxypiperidin-1-yl)sulfonyl]-3-thienyl}-4-methyl-1,3-thiazol-2-yl)acetamide as an oil (31 mg; 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399497B2
Source datasetuspto-grants-2013_03
ORD IDord-2b86b4381ac84e5085d3c70ad1b31e87
Source noteuspto-grants-2013_03