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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112951Generated: October 31, 2026

[2-(Dimethylamino)pyrimidin-5-yl]boronic acid → 2-Amino-7-(2-dimethylamino-pyrimidin-5-yl)-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid hydrazide

https://huagongshe.com/reaction/2112951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(Dimethylamino)pyrimidin-5-yl]boronic acidHCID 45088929—
Reactant2-Amino-7-bromo-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid ethyl esterHCID 57643072—
Reactant2-Amino-7-(2-dimethylamino-pyrimidin-5-yl)-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid ethyl esterHCID 57643148—
Product2-Amino-7-(2-dimethylamino-pyrimidin-5-yl)-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid hydrazideHCID 57643123—

Reaction Steps

2-Amino-7-(2-dimethylamino-pyrimidin-5-yl)-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid ethyl ester, was prepared analogously to Example 28, Step 3, except 2-amino-7-bromo-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid ethyl ester (10.0 g, 35.1 mmol) was used as the starting material (which may be prepared as described in Example 6) and 2-dimethylamino-pyrimidin-5-boronic acid was used in place of 3-pyridyl-boronic acid to give 2-amino-7-(2-dimethylamino-pyrimidin-5-yl)-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid hydrazide. MS (APCI+): m/z 328.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524860B2
Source datasetuspto-grants-2009_04
ORD IDord-7679afdfa2ba418080a8aa62250b9779
Source noteuspto-grants-2009_04