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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008643Generated: November 2, 2026

Tetrahydrofuran → HCID 21962397, compound

https://huagongshe.com/reaction/1008643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21962345HCID 21962345—
SolventMethanolHCID 887—
ProductHCID 21962397HCID 2196239793.2%

Reaction Steps

Ethyl 4-{2-[1-benzhydryl-5-chloro-2-(2-{[(3,4-dichlorobenzyl)sulfonyl]amino)-ethyl)-1H-indol-3-yl]ethoxy}-2-fluorobenzoate (0.11 g, 0.14 mmol), THF (0.5 mL), MeOH (0.5 mL), and 1 N NaOH (0.5 mL) were stirred together overnight. Solvents were removed and the resulting residue was taken up in water. The solution was acidified with 1N HCl and extracted with ethyl acetate. The extract was dried over sodium sulfate, and evaporated. The resulting residue was triturated with a mixture of ether and hexanes to give 0.10 g of 4-{2-[1-benzhydryl-5-chloro-2-(2-{[(3,4-dichlorobenzyl)sulfonyl]amino}ethyl)-1H-indol-3-yl]ethoxy}-2-fluorobenzoic acid as a white solid; mp 117-119° C.; HRMS: calcd for C39H32Cl3FN2O5S, 764.1082; found (ESI+), 787.09794

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797708B2
Source datasetuspto-grants-2004_09
ORD IDord-9403510644b44dd79acb176de5ee597f
Source noteuspto-grants-2004_09