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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530663Generated: November 3, 2026

Lithium Chloride → 12-(1-ethoxyethenyl)-13-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca1(14),2,4,10,12-pentaene

https://huagongshe.com/reaction/1530663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
ReactantPotassium FluorideHCID 522689—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant12-bromo-13-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca1(14),2,4,10,12-pentaeneHCID 68313180—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product12-(1-ethoxyethenyl)-13-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca1(14),2,4,10,12-pentaeneHCID 6831291968%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 12-bromo-13-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca1(14),2,4,10,12-pentaene (1.0 g, 2.6 mmol), tributyl(1-ethoxyvinyl)stannane (1.2 mL), Pd(PPh3)4 (90 mg, 7.8 mmol), and LiCl (328 mg, 7.8 mmol) in dry THF (10 mL) was stirred at 70° C. for 48 h under nitrogen atmosphere. KF (100 mL, 0.16 M) was added and the mixture was further stirred at room temperature for 1 h. The solid was filtered off. The filtrate was concentrated to give the crude product, which was purified by reverse phase Combiflash eluting with a 0-50% gradient of CH3CN in 0.3% NH4HCO3 to afford 12-(1-ethoxyethenyl)-13-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca1(14),2,4,10,12-pentaene (660 mg, 68% yield). LCMS (ESI) m/z: 380.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-fd54d4dc50c148b6bf2baf6d8db252f8
Source noteuspto-grants-2015_07