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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873982Generated: October 31, 2026

4-Chlorobenzaldehyde → 5-(4-chlorophenyl)-4-(cyclopropanecarbonyl)-1-(3,8-dimethyl-[1,2,4]triazolo[4,3-a]-pyridin-6-yl)-3-hydroxy-1H-pyrrol-2(5H)-one

https://huagongshe.com/reaction/873982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantEthyl 4-cyclopropyl-2,4-dioxobutanoateHCID 16779961—
Reactant3,8-Dimethyl-[1,2,4]triazolo[4,3-a]pyridin-6-amineHCID 75357449—
Product5-(4-chlorophenyl)-4-(cyclopropanecarbonyl)-1-(3,8-dimethyl-[1,2,4]triazolo[4,3-a]-pyridin-6-yl)-3-hydroxy-1H-pyrrol-2(5H)-oneHCID 117702627—

Reaction Steps

The title compound was prepared in analogy to the procedure described in Step 84.5 using 3,8-dimethyl-[1,2,4]triazolo[4,3-a]pyridin-6-amine (Step 67.4), 4-chlorobenzaldehyde and ethyl 4-cyclopropyl-2,4-dioxobutanoate. tR: 0.82 min (LC-MS 2); ESI-MS: 483 [M+H]+ (LC-MS 2); 1H NMR (400 MHz, DMSO-d6) δ ppm 0.60-0.97 (m, 4H) 2.41 (s, 3H) 2.55-2.68 (m, 3H) 2.85-2.93 (m, 1H) 6.12 (s, 1H) 7.11-7.28 (m, 2H) 7.28-7.41 (m, 3H) 8.50 (s, 1H) —OH missing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975417B2
Source datasetuspto-grants-2015_03
ORD IDord-0d54cc18b43b414e821c1073f8afb011
Source noteuspto-grants-2015_03