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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088709Generated: November 1, 2026

Water → (4-{5-[(2-{[6-Amino-5-(trifluoroacetyl)pyridin-2-yl]amino}ethyl)amino]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-yl}piperidin-1-yl)acetic acid

https://huagongshe.com/reaction/2088709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 70249298HCID 70249298—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(4-{5-[(2-{[6-Amino-5-(trifluoroacetyl)pyridin-2-yl]amino}ethyl)amino]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-yl}piperidin-1-yl)acetic acidHCID 67228276—

Reaction Steps

130 mg (0.19 mmol) of ethyl(4-{5-[(2-{[6-amino-5-(trifluoroacetyl)pyridin-2-yl]amino}ethyl)-amino]-7-(2,4-dichlorophenyl)[1,2,4]triazolo[1,5-c]pyrimidin-2-yl}piperidin-1-yl)acetate (Example 56A) were dissolved in 1,2-dimethoxyethane (7.5 ml), water (5 ml) and 31 mg (0.76 mmol) of sodium hydroxide were added and the reaction mixture was stirred at RT for 16 h. The mixture was then concentrated by lyophilization. This gave, after purification of the residue by preparative HPLC (Method 11), 60 mg (48% of theory) of the product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436003B2
Source datasetuspto-grants-2013_05
ORD IDord-b5d4376090834114bb891bea48115827
Source noteuspto-grants-2013_05