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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233936Generated: October 30, 2026

2,4-Dichloro-6-methoxy-3,5-triazine → 3,4-Dichloro-N-[1-(4-chloro-6-methoxy-1,3,5-triazin-2-yl)piperidin-4-yl]-5-methyl-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/2233936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6-methoxy-3,5-triazineHCID 19267—
ReactantHCID 68579996HCID 68579996—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3,4-Dichloro-N-[1-(4-chloro-6-methoxy-1,3,5-triazin-2-yl)piperidin-4-yl]-5-methyl-1H-pyrrole-2-carboxamideHCID 86608286—

Reaction Steps

A solution of 2,4-dichloro-6-methoxy-1,3,5-triazine (commercially available) (0.05 g, 0.32 mmol) in DMF (0.5 ml) was added to a solution of 3,4-dichloro-5-methyl-N-piperidin-4-yl-1H-pyrrole-2-carboxamide hydrochloride (Intermediate 1, 0.1 g, 0.32 mmol) and TEA (0.06 g, 0.64 mmol) in DMF (1.5 ml). The resultant mixture was stirred for 1 h at room temperature, then was diluted with water and extracted with EtOAc. During the aqueous workup, some of the product precipitated and was collected by suction filtration. The organic extract was dried over magnesium sulphate, filtered and concentrated to give the desired product with small amount of impurities.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-c990d5f92f9d4f1cb7355c4ad80f37b4
Source noteuspto-grants-2010_05