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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088706Generated: November 2, 2026

Diisopropylethylamine → 1-[2-Amino-6-({1-[2-(1-cyclopropylpiperidin-4-yl)-7-(2,4-dichlorophenyl)[1,2,4]triazolo[1,5-c]-pyrimidin-5-yl]piperidin-3-yl}amino)pyridin-3-yl]propan-1-one

https://huagongshe.com/reaction/2088706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67228770HCID 67228770—
ReactantHCID 86654417HCID 86654417—
SolventDimethyl SulfoxideHCID 679—
Product1-[2-Amino-6-({1-[2-(1-cyclopropylpiperidin-4-yl)-7-(2,4-dichlorophenyl)[1,2,4]triazolo[1,5-c]-pyrimidin-5-yl]piperidin-3-yl}amino)pyridin-3-yl]propan-1-oneHCID 67229311—

Reaction Conditions

Temperature120 °C

Reaction Steps

25 mg (0.06 mmol) of 5-chloro-7-(2,4-dichlorophenyl)-2-(1-cyclopropylpiperidin-4-yl)-[1,2,4]-triazolo[1,5-c]pyrimidine hydrochloride, 20 mg (0.07 mmol) of 1-[2-amino-6-(piperidin-3-ylamino)pyridin-3-yl]propan-1-one hydrochloride (Example 27A) and 65 μl (0.4 mmol) of N,N-diisopropylethylamine were initially charged in 1.25 ml of DMSO. The mixture was heated in the microwave at 120° C. for 30 min. This gave, after purification of the crude product by preparative HPLC (Method 11), 21 mg (56% 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-510a0b27064c400888b31ee689de0d83
Source noteuspto-grants-2013_05