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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048533Generated: October 31, 2026

2-Thiophenesulfonamide → HCID 67999458, compound

https://huagongshe.com/reaction/1048533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenesulfonamideHCID 72881—
ReactantCyanomethylenetributylphosphoraneHCID 4622928—
ReactantHCID 67999735HCID 67999735—
SolventTolueneHCID 1140—
ProductHCID 67999458HCID 67999458—

Reaction Conditions

Temperature35 °C

Reaction Steps

To a solution of methyl 2-((3R,5R,6S)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((S)-1-cyclopropyl-2-hydroxyethyl)-3-methyl-2-oxopiperidin-3-yl)acetate (100 mg, 0.184 mmol; Example 263, Step C) and cyanomethylenetributylphosphorane (177 μL, 0.734 mmol) in toluene (0.92 mL) was added thiophene-2-sulfonamide (90 mg, 0.55 mmol) and the resulting solution was stirred at 35° C. overnight. The reaction was quenched (sat. NH4Cl), extracted (2×EtOAc), and washed (brine). The combined organic layers were dried (Na2SO4) and concentrated under the reduced pressure. Purification of the residue by chromatography on silica gel (24 g SiO2, 35% EtOAc/Hex) provided the title compound as a pale yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-fa049b4e1b934cf3ad6165ca77eed6ef
Source noteuspto-grants-2013_10