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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751394Generated: October 28, 2026

Potassium Carbonate → (1S,3R)-tert-butyl 3-(6-(8-chloro-6H-benzo[c]chromen-3-yl)-1H-benzo[d]imidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate

https://huagongshe.com/reaction/1751394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Azabicyclo(2.2.1)heptane-2-carboxylic acid, 3-(6-bromo-1H-benzimidazol-2-yl)-, 1,1-dimethylethyl ester, (1R,3S,4S)-HCID 67505868—
Reactant2-(8-chloro-6H-benzo[c]chromen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 69675282—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(1S,3R)-tert-butyl 3-(6-(8-chloro-6H-benzo[c]chromen-3-yl)-1H-benzo[d]imidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylateHCID 8670872725%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 2-(8-chloro-6H-benzo[c]chromen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (750 mg, 2.18 mmol), (1R,3S,4S)-tert-butyl 3-(6-bromo-1H-benzo[d]imidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate (1.07 mg, 2.72 mmol), tetrakis(triphenylphosphine) palladium(0) (75 mg, 0.07 mmol) and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) (96 mg, 0.13 mmol) in a mixture of 1,2-dimethoxyethane (10 mL) and dimethylformamide (2 mL) was added a solution of potassium carbonate (2M in water, 3.5 mL, 6.53 mmol). The resulting mixture was degassed and then heated to 85° C. under argon for 18 hours. After cooling to room temperature, the reaction was diluted with ethyl acetate. The organics were washed with water and brine, dried (Na2SO4), and concentrated. The crude residue was purified by flash chromatography to yield (1S,3R)-tert-butyl 3-(6-(8-chloro-6H-benzo[c]chromen-3-yl)-1H-benzo[d]imidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate (285 mg, 25%) LCMS-ESI+: calculated for C31H30ClN3O3: 528.06; observed [M+1]+: 528.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-2381d3ab15ac418984768ec56194cd62
Source noteuspto-grants-2015_10