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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019548Generated: October 30, 2026

2-Chloropyrimidin-5-amine → N-(2-Chloropyrimidin-5-yl)-5-trifluoromethyl-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxamide

https://huagongshe.com/reaction/1019548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloropyrimidin-5-amineHCID 12215993—
Reactant5-Trifluoromethyl-1-[(3-fluorophenyl)methyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acidHCID 66863517—
ProductN-(2-Chloropyrimidin-5-yl)-5-trifluoromethyl-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxamideHCID 8663906122.9%

Reaction Steps

According to a method similar to that described in Stage 1.4, starting from 1.08 g (3.2 mmol) of 5-trifluoromethyl-1-[(3-fluorophenyl)methyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, described in Stage 1.3, and 0.46 g (3.52 mmol) of 2-chloro-5-aminopyrimidine, we obtain 0.33 g of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716272B2
Source datasetuspto-grants-2014_05
ORD IDord-5def9331bd0b4571be496bf7614949f3
Source noteuspto-grants-2014_05