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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715692Generated: November 1, 2026

3-Amino-1-propanol → N-(3-hydroxypropyl)-4-({4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}amino)benzenesulfonamide

https://huagongshe.com/reaction/1715692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-1-propanolHCID 9086—
Reactant4-({4-[4-(Trifluoromethyl)phenyl]pyrimidin-2-yl}amino)benzenesulfonyl chlorideHCID 86604282—
SolventEthyl AcetateHCID 8857—
ProductN-(3-hydroxypropyl)-4-({4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}amino)benzenesulfonamideHCID 6867331588.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-({4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}amino)benzenesulfonyl chloride (0.10 g, 0.25 mmol) in 2 ml of ethyl acetate is added 3-amino-1-propanol (0.19 g, 2.5 mmol) with stirring, at 0° C. The mixture is stirred at room temperature for 1 hr and then quenched with water (10 ml). The ethyl acetate is evaporated, the resulting suspension is filtered, and the precipitate is washed with water, and hexanes, and then dried in vacuo to give 0.10 g of a white solid; mp 204-205° C.; HRMS: calcd for C20H19F3N4O3S, 452.1130; found (ESI-FTMS, [M+H]1+), 453.12161.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799915B2
Source datasetuspto-grants-2010_09
ORD IDord-ce82a455118041a1bba8380dca4d4443
Source noteuspto-grants-2010_09