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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253164Generated: October 25, 2026

Potassium Carbonate → (2S)-2,3-dihydro-1-[(3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-yl)sulfonyl]indole-2-carboxylic acid

https://huagongshe.com/reaction/253164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIndoline-2-carboxylic acid, (S)-HCID 2733920—
Reactant2,2-Dimethyl-6-Chromanesulfonyl ChlorideHCID 2779774—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(2S)-2,3-dihydro-1-[(3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-yl)sulfonyl]indole-2-carboxylic acidHCID 6684581173%

Reaction Steps

1 g (6.13 mmol) of 2,3-dihydro-(2S)-1H-indole-2-carboxylic acid, and 0.97 g (7.05 mmol) of potassium carbonate are solubilised in 2 ml of water. 1.6 g (6.13 mmol) of 3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-sulfonyl chloride solubilised in 12 ml of acetonitrile and 2 ml of water are added. Agitation is allowed to take place for 5 hours at ambient temperature. Water is added to the reaction medium, washing is performed with ethyl acetate, the acidity of the aqueous phase is raised to pH 3 by a solution of hydrochloric acid 1 N, and then extraction is performed using ethyl acetate. The organic phases are collected, dried on magnesium sulfate, filtered and concentrated under reduced pressure. The evaporation residue is purified by silica column chromatography eluting with the help of a dichloromethane/methanol (9/1; v/v) mixture. The expected product is obtained in the form of a beige foam with a yield of 73%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872021B2
Source datasetuspto-grants-2011_01
ORD IDord-2219d297833a45b8bd1d6439377e0d1c
Source noteuspto-grants-2011_01