Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874434Generated: October 30, 2026

Dichloromethane → N-(2-bromo-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-7-yl)-1-methyl-4-(6-methylpyridin-2-yl)-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/874434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium BicarbonateHCID 516892—
Reactant1-methyl-4-(6-methylpyridin-2-yl)-1H-pyrazole-5-carbonyl chlorideHCID 90383457—
Reactant2-Bromo-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-7-amine hydrochlorideHCID 117761201—
SolventTriethylamineHCID 8471—
ProductN-(2-bromo-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-7-yl)-1-methyl-4-(6-methylpyridin-2-yl)-1H-pyrazole-5-carboxamideHCID 9038344446.9%

Reaction Steps

The 2-bromo-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-7-amine hydrochloride (38 mg) obtained in (Example 5.16) <Step 6> was added at 0° C. to a methylene chloride (1 ml) solution of the 1-methyl-4-(6-methylpyridin-2-yl)-1H-pyrazole-5-carbonyl chloride (35 mg) obtained in (Example 5.47) <Step 1> and triethylamine (0.06 ml). The obtained mixture was stirred for 30 minutes. Thereafter, a saturated sodium hydrogen carbonate aqueous solution (2 ml) was added to the reaction solution, and the mixed solution was then purified by LC/MS, so as to obtain the title compound (29 mg) in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980889B2
Source datasetuspto-grants-2015_03
ORD IDord-ef80c418b7794b338d26d3a0223b3676
Source noteuspto-grants-2015_03