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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556486Generated: October 30, 2026

1,4-Dioxane → HCID 57479120, compound

https://huagongshe.com/reaction/556486

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant2-[(3-chlorophenyl)amino]acetic AcidHCID 3780319—
Reactant3-Bromo-6-chloro-3-(3-chloro-benzyl)-1,3-dihydro-indol-2-oneHCID 57507273—
SolventPotassium CarbonateHCID 11430—
ProductHCID 57479120HCID 5747912037.1%

Reaction Steps

At room temperature, (3-Chloro-phenylamino)-acetic acid (1.25 g, 6.8 mmol) was dissolved in 10 ml 1N K2CO3 aqueous solution, then 3-Bromo-6-chloro-3-(3-chloro-benzyl)-1,3-dihydro-indol-2-one (2.5 g, 6.8 mmol) and 10 ml 1,4-dioxane were added slowly. After stirred for about 3 h, the solution was concentrated and the water layer was extracted with CH2Cl2. The organic layer was dried, concentrated to obtain the crude product and the crude product was purified by chromatography to obtain 1.2 g yellow solid rac-[[6-Chloro-3-(3-chloro-benzyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-(3-chloro-phenyl)-amino]-acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058269B2
Source datasetuspto-grants-2011_11
ORD IDord-754096abfd684783b832a8269d148724
Source noteuspto-grants-2011_11