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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047187Generated: November 1, 2026

HCID 58173379, compound → HCID 58173414, compound

https://huagongshe.com/reaction/2047187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58173379HCID 58173379—
ReactantHCID 66733403HCID 66733403—
ReactantHCID 66733508HCID 66733508—
ProductHCID 58173414HCID 58173414—

Reaction Steps

(4-(7-Amino-6-chloro-3-(quinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)piperazin-1-yl)(thiophen-2-yl)methanone was synthesized in a manner similar to the synthesis of (4-(7-amino-6-bromo-3-(quinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)-5,6-dihydropyridin-1(2H)-yl)(thiophen-2-yl)methanone, but with 6-chloro-5-(piperazin-1-yl)-3-(quinolin-3-yl)pyrazolo[1,5-a]pyrimidin-7-amine substituted for 6-bromo-3-(quinolin-3-yl)-5-(1,2,3,6-tetrahydropyridin-4-yl)pyrazolo[1,5-a]pyrimidin-7-amine. The reaction was purified via reverse-phase preparatory HPLC to yield (4-(7-amino-6-chloro-3-(quinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)piperazin-1-yl)(thiophen-2-yl)methanone as yellow solid. (M+H=490.19, retention time=3.75 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08591943B2
Source datasetuspto-grants-2013_11
ORD IDord-e4a358e5adc24e11a706ccd19ebd9c4e
Source noteuspto-grants-2013_11