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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467802Generated: October 26, 2026

Dichloromethane → Benzyl 4-(4-chloro-5-trifluoromethylpyrimidin-2-ylamino)-benzoate

https://huagongshe.com/reaction/467802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl p-aminobenzoateHCID 98488—
Reactant2,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 2782774—
SolventDimethylacetamideHCID 31374—
ProductBenzyl 4-(4-chloro-5-trifluoromethylpyrimidin-2-ylamino)-benzoateHCID 58809948—

Reaction Conditions

Temperature60 °C

Reaction Steps

10 g (44 mmol) benzyl 4-aminobenzoate are dissolved in 200 mL DMA, 8 mL Hünig base (0.97 eq) are added and 10.4 g (48.21 mmol) 2,4-dichloro-5-trifluoromethylpyrimidine, dissolved in 50 mL DMA, are added dropwise at RT to this solution. The reaction mixture is stirred at 60° C. overnight, then combined with 300 mL DCM and extracted with water (3 times 300 mL). The organic phase is dried and the solvent is eliminated in vacuo. The crude product is combined with 100 mL MeOH, digested and left to stand for 2 h. Then it is stirred for 10 min, the precipitate is filtered off and washed with MeOH. Finally the crude product is again suspended in MeOH, filtered off, washed with a little MeOH and dried in the vacuum dryer at 60° C. 8.5 g A-2a are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623887B2
Source datasetuspto-grants-2014_01
ORD IDord-8a32d504900b462eb107f58c27390590
Source noteuspto-grants-2014_01