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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400457Generated: October 30, 2026

Phenylboronic Acid → 3-Phenyl-5,6,8,9-tetrahydro-1,2,7-triaza-benzocycloheptene-7-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/400457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant3-Chloro-5,6,8,9-tetrahydro-1,2,7-triaza-benzocycloheptene-7-carboxylic acid tert-butyl esterHCID 86686055—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-Phenyl-5,6,8,9-tetrahydro-1,2,7-triaza-benzocycloheptene-7-carboxylic acid tert-butyl esterHCID 86686054149.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

5 g phenylboronic acid in 30 mL dioxane was added to 3.2 g 3-chloro-5,6,8,9-tetrahydro-1,2,7-triaza-benzocycloheptene-7-carboxylic acid tert-butyl ester and 388 mg (1,1′-bis(diphenyl-phosphinoferrocene)palladium(II)dichloride in 50 mL dioxane under argon. The reaction was stirred at 90° C. over night. The mixture was cooled to RT diluted with water and extracted with ethyl acetate. The organic layer was washed with aqueous sodium hydroxide and brine. The solvent was removed and the precipitate was purified by column chromatographie to yield 5.5 g of the desired product. (M+H)+=325

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741892B2
Source datasetuspto-grants-2014_06
ORD IDord-bca653d621e94bfebe6da733e094c1a2
Source noteuspto-grants-2014_06