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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615923Generated: November 1, 2026

HCID 66785913, compound → HCID 71735754, compound

https://huagongshe.com/reaction/1615923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66785913HCID 66785913—
ReactantHCID 86696517HCID 86696517—
ProductHCID 71735754HCID 7173575435.3%

Reaction Steps

A mixture of 8-chloro-3-(cyclopropyl methyl)-7-iodo-[1,2,4]triazolo[4,3-a]pyridine (60 mg, 0.180 mmol), 2-(2-(aminomethyl)cyclopropyl)benzonitrile (31.0 mg, 0.180 mmol) was reacted in a manner similar to Example 1 to give 2-(2-(((8-chloro-3-(cyclopropylmethyl)-[1,2,4]triazolo[4,3-a]pyridin-7-yl)amino)methyl)cyclopropyl)benzonitrile (24 mg, 32.5%) as a film. 1H NMR (400 MHz, METHANOL-d4) δ 8.15 (d, J=7.5 Hz, 1H), 7.62 (dd, J=7.8, 1.0 Hz, 1H), 7.53 (td, J=7.8, 1.3 Hz, 1H), 7.29 (td, J=7.7, 1.0 Hz, 1H), 7.11 (d, J=8.0 Hz, 1H), 6.97 (d, J=7.8 Hz, 1H), 3.65 (dd, J=14.6, 6.0 Hz, 1H), 3.51 (dd, J=14.6, 6.5 Hz, 1H), 2.98 (d, J=6.8 Hz, 2H), 2.28-2.20 (m, 1H), 1.55 (ddd, J=8.7, 6.1, 4.8 Hz, 1H), 1.26-1.08 (m, 3H), 0.65-0.54 (m, 2H), 0.36-0.25 (m, 2H). LCMS: M+1=378.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765767B2
Source datasetuspto-grants-2014_07
ORD IDord-33597314fe454d1c9376a8f1d8f6a6fe
Source noteuspto-grants-2014_07