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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603971Generated: October 30, 2026

Dichloromethane → HCID 21962365, compound

https://huagongshe.com/reaction/603971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Chlorophenyl)methanesulfonyl chlorideHCID 2757801—
ReactantHCID 21962279HCID 21962279—
SolventWaterHCID 962—
ProductHCID 21962365HCID 21962365—

Reaction Steps

[(2-chlorophenyl)methyl]sulfonyl chloride (0.14 g, 0.6 mmol) was added to a mixture of ethyl 4-{2-[2-(2-Aminoethyl)-1-benzhydryl-5-chloro-1H-indol-3-yl]-ethoxy}-2-fluoro-benzoate (Step 6, Example 190, 0.12 g, 0.2 mmol) and K2CO3 (0.11 g, 0.8 mmol) in CH2Cl2 (2 mL) and water (1 mL) with stirring. After 2 hour at room temperature, the mixture was extracted with CH2Cl2 (10 mL) and the extract was washed with 0.5 N NaOH, and brine and dried over sodium sulfate. The CH2Cl2 solution was filtered through silica gel and the filtrate was evaporated. The resulting residue was triturated with a mixture of ether and hexanes to give 0.07 g of ethyl 4-{2-[1-benzhydryl-5-chloro-2-(2-{[(2-chlorobenzyl)sulfonyl]amino}ethyl)-1H-indol-3-yl]ethoxy}-2-fluorobenzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906548B2
Source datasetuspto-grants-2011_03
ORD IDord-6982a4c101a54565b07d49d82dacc9b6
Source noteuspto-grants-2011_03