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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774466Generated: November 2, 2026

5-Aminosalicylic Acid → HCID 71243638, compound

https://huagongshe.com/reaction/1774466

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminosalicylic AcidHCID 4075—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 71243533HCID 71243533—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71243638HCID 7124363830.2%

Reaction Steps

To a mixture of ethyl 4-(((1R,2R)-1-hydroxy-2,3-dihydro-1H,1′H-[2,2′-biinden]-2-yl)methyl)benzoate (11, 200 mg, 0.48 mmol), 5-amino-2-hydroxybenzoic acid (75 mg, 0.48 mmol) and THF (1.0 mL) in a 5 mL microwave vial, was added trimethylaluminium (0.5 mL, 20% solution in toluene) and the mixture irradiated at 100° C. for 5 min. The reaction mixture was quenched with slow addition of 1.5 N HCl (2 mL) and extracted with ethyl acetate (3×15 mL). Organic layer was washed with water (25 mL), brine (25 mL), dried over anhydrous Na2SO4 and evaporated under reduced pressure. The residue purified by preparative HPLC [Kromasil C18 (250×50 mm), flow rate: 40 mL/min, 0.1% TFA in water/MeOH, run time: 40 min] to yield 75 mg (30%) of the title compound as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260376B2
Source datasetuspto-grants-2016_02
ORD IDord-1d75acdd0bcf4b519373afea5472b97d
Source noteuspto-grants-2016_02