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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216042Generated: October 25, 2026

Pyridine → HCID 67036917, compound

https://huagongshe.com/reaction/216042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzenesulfonamide, 3-amino-HCID 7377—
ReactantOxalyl chlorideHCID 65578—
Reactant1-[(Tert-butoxy)carbonyl]-4-methylpiperidine-4-carboxylic acidHCID 23282848—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 67036917HCID 6703691740%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1-(tert-butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid (60 mg, 0.25 mmol) in dichloroethane (2.0 mL) were added DMF (2 drops) and pyridine (78 mg, 0.99 mmol), followed by oxalyl chloride (31 mg, 0.25 mmol). The mixture was stirred for 40 minutes, and 3-amino-benzenesulfonamide was added. The mixture was heated at 50° C. for 3 hours, and the mixture was cooled, diluted with dichloromethane, washed twice each with sat. aq. NaHCO3 and 1.0 N aq. HCl, dried over MgSO4, and concentrated. Silica gel chromatography (2-5% MeOH:CH2Cl2) gave the title compound in 40% yield. MS (ES+) [M+H]+=398.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193202B2
Source datasetuspto-grants-2012_06
ORD IDord-6035889bb3d04fada903cdea369cbbe9
Source noteuspto-grants-2012_06