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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273071Generated: October 30, 2026

Sodium Carbonate → HCID 89714886, compound

https://huagongshe.com/reaction/2273071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantHCID 59578631HCID 59578631—
ReactantHCID 89714606HCID 89714606—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 89714886HCID 89714886—

Reaction Conditions

Temperature90 °C

Reaction Steps

1.77 g (5.85 mmol) of 4-chloro-6-ethyl-8,8-dimethyl-2-methylsulfanyl-7,8-dihydro-6H-9-oxa-1,3,6-triazabenzocyclohepten-5-one, 2.27 g (6.73 mmol) of [3-fluoro-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl]carbamic acid tert-butyl ester and 14.63 ml of a 2 M solution of Na2CO3 in 35 ml dioxane are mixed together, followed by degassing 5 times with argon. 339 mg (293 μmol) of tetrakis(triphenylphosphine)palladium (0) are added and the mixture is degassed a further 3 times with argon and then heated at 90° C. for 2 hours 30 minutes. The resulting mixture is allowed to cool. It is poured into water. The product is filtered off, washed with water, dissolved in DCM, dried and concentrated. It is taken up in Et2O, and the mixture is stirred, filtered and dried. 2.94 g of [4-(6-ethyl-8,8-dimethyl-2-methylsulfanyl-5-oxo-5,6,7,8-tetrahydro-9-oxa-1,3,6-triazabenzocyclo hepten-4-yl)-3-fluorophenyl]carbamic acid tert-butyl ester are recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120812B2
Source datasetuspto-grants-2015_09
ORD IDord-c4ff609c115948698179c438f97570a9
Source noteuspto-grants-2015_09