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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047196Generated: November 1, 2026

HCID 58173379, compound → HCID 58173458, compound

https://huagongshe.com/reaction/2047196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58173379HCID 58173379—
ReactantHCID 66733403HCID 66733403—
Reactant6-Chloro-3-(quinolin-3-yl)-5-(1,2,3,6-tetrahydropyridin-4-yl)pyrazolo[1,5-a]pyrimidin-7-amineHCID 67494268—
ProductHCID 58173458HCID 58173458—

Reaction Steps

(4-(7-amino-6-chloro-3-(quinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)-5,6-dihydropyridin-1(2H)-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-3-(quinolin-3-yl)-5-(1,2,3,6-tetrahydropyridin-4-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 mixture 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)-5,6-dihydropyridin-1(2H)-yl)(thiophen-2-yl)methanone as yellow solid. (m+H=487.17, retention time=3.73 min)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08591943B2
Source datasetuspto-grants-2013_11
ORD IDord-5e4e99a5dfbd44ee8895fb1873b8cb33
Source noteuspto-grants-2013_11