Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696123Generated: October 26, 2026

Dabco → N-(pyrimidin-4-yl)-4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzenesulfonamide

https://huagongshe.com/reaction/1696123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDabcoHCID 9237—
Reactant4-AminopyrimidineHCID 68958—
Reactant4-(1-(2,2,2-Trifluoroacetyl)piperidin-4-yl)benzene-1-sulfonyl chlorideHCID 17973478—
SolventAcetonitrileHCID 6342—
ProductN-(pyrimidin-4-yl)-4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzenesulfonamideHCID 5946587336.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

Prepared using general procedure 15, method B. Prepared using a mixture of 4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzene-1-sulfonyl chloride (2.0 g, 5.6 mmol), 4-aminopyrimidine (535 mg, 5.6 mmol), DABCO (3.1 g, 28.0 mmol) and acetonitrile (10 mL). The reaction mixture was heated at 40° C. for 6 h. Purification via silica gel chromatography using 5% MeOH in CH2Cl2 gave N-(pyrimidin-4-yl)-4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzenesulfonamide (850 mg, 36%). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=415.3; tR=2.57 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163720B2
Source datasetuspto-grants-2012_04
ORD IDord-5bcf952db2b642029ee57ef54df2cda6
Source noteuspto-grants-2012_04