Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530581Generated: November 2, 2026

2-Iodobenzoic acid → 12-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca-1(14),2,4,10,12-pentaene-13-carbaldehyde

https://huagongshe.com/reaction/1530581

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodobenzoic acidHCID 6941—
ReactantHCID 68312830HCID 68312830—
SolventEthyl AcetateHCID 8857—
Product12-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca-1(14),2,4,10,12-pentaene-13-carbaldehydeHCID 8667146871.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of {12-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca-1(14),2,4,10,12-pentaen-13-yl}methanol (92 mg, 0.271 mmol) in EtOAc (10 mL) was added 2-iodobenzoic acid (304 mg, 1.086 mmol). The mixture was heated at 80° C. overnight. The solid was filtered, the filtrate was concentrated and purified by silica gel chromatography eluting with EtOAc/petroleum ether (1:1) to give 12-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca-1(14),2,4,10,12-pentaene-13-carbaldehyde (65 mg, 71% yield) as a yellow solid. LCMS (ESI) m/z: 338.1 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-5a512befcf084eaa8065ed8ccecb5520
Source noteuspto-grants-2015_07