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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591009Generated: October 30, 2026

Water → methyl 2-(tert-butoxy)-2-[3-(3,4-dihydro-2H-1-benzopyran-6-yl)thieno[2,3-b]pyridin-2-yl]acetate

https://huagongshe.com/reaction/591009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-(3,4-dihydro-2H-1-benzopyran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 43811034—
ReactantMethyl 2-{3-bromothieno[2,3-b]pyridin-2-yl}-2-(tert-butoxy)acetateHCID 70855404—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDimethylformamideHCID 6228—
Productmethyl 2-(tert-butoxy)-2-[3-(3,4-dihydro-2H-1-benzopyran-6-yl)thieno[2,3-b]pyridin-2-yl]acetateHCID 7085540749%

Reaction Conditions

Temperature110 °C

Reaction Steps

Under a nitrogen atmosphere, sodium carbonate (16 mg, 0.15 mmol), water (1 mL), palladium tetrakis(triphenylphosphine) (27 mg, 0.02 mmol) and 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)chroman (40 mg, 0.15 mmol) were added to a solution of methyl 2-{3-bromothieno[2,3-b]pyridin-2-yl}-2-(tert-butoxy)acetate (14g) (55 mg, 0.15 mmol) in N,N-dimethylformamide (4 mL). The mixture was heated at 110° C. for 1 hour. The mixture was then cooled at room temperature, concentrated and water (20 mL) was added. The aqueous layer was extracted with ethyl acetate (2×20 mL). The organic layer was washed with brine (20 mL), dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (dichloromethane/ethyl acetate 90/10) to afford the desired product (14h) as a white solid (30 mg, 0.07 mmol, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-a3c273093bd7468c81dff10f0aee832e
Source noteuspto-grants-2016_01