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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728098Generated: October 30, 2026

Water → HCID 76568006, compound

https://huagongshe.com/reaction/1728098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantHCID 76567867HCID 76567867—
CatalystWaterHCID 962—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 76568006HCID 7656800638.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

Under Argon atmosphere, racemic (2′R,3R,4′S)-6-bromo-4′-(3-chlorophenyl)-2′-(1-ethyl-cyclopropyl)-2,3-dihydro-2,6′-dioxospiro[indole-3,3′-piperidine]-1-carboxylic acid tert-butyl ester (28 mg, 0.049 mmol), cyclopropylboronic acid (4.5 mg, 0.0524 mmol), Pd(PPh3)4 (5 mg), K3PO4 (50 mg) and a few drops of water were mixed in toluene (3 mL). The mixture was heated under microwave irradiation at 130° C. for 20 min. Then the solution was poured into water and the aqueous layer was extracted with EtOAc. The organic layer was dried and concentrated. The residue was purified by Prep-TLC to obtain racemic (2′R,3R,4′S)-6-cyclopropyl-4′-(3-chlorophenyl)-2′-(1-ethyl-cyclopropyl)-2,3-dihydro-2,6′-dioxospiro[indole-3,3′-piperidine]-1-carboxylic acid tert-butyl ester (10 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-f57e32cbfc134bf88245fdf919715504
Source noteuspto-grants-2009_02