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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200056Generated: November 2, 2026

HCID 117728990, compound → Methanesulfonic acid 2-{3-[3-(cyano-dimethyl-methyl)-5-(3-{(1S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-ureido)-pyrazol-1-yl]-phenoxy}-ethyl ester

https://huagongshe.com/reaction/2200056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117728990HCID 117728990—
Reactant1-{5-(Cyano-dimethyl-methyl)-2-[3-(2-hydroxy-ethoxy)-phenyl]-2H-pyrazol-3-yl}-3-{(1S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-ureaHCID 117729326—
ProductMethanesulfonic acid 2-{3-[3-(cyano-dimethyl-methyl)-5-(3-{(1S,4R)-4-[3-((2S,6R)-2,6-dimethyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-ureido)-pyrazol-1-yl]-phenoxy}-ethyl esterHCID 117729092—

Reaction Steps

The title compound was prepared using Intermediate 21a in an analogous fashion to the procedures described for Intermediate A step e. LCMS (Method 3): Rt 3.85 min, m/z 782.5 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359354B2
Source datasetuspto-grants-2016_06
ORD IDord-20dc621dd10a4b8d82b58e3a1192e455
Source noteuspto-grants-2016_06