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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212776Generated: October 31, 2026

Tetrahydrofuran → HCID 21962498, compound

https://huagongshe.com/reaction/2212776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21962452HCID 21962452—
SolventMethanolHCID 887—
ProductHCID 21962498HCID 2196249893.9%

Reaction Steps

Ethyl 3-[4-({2-[1-benzhydryl-5-chloro-2-(2-{[(3,4-dichlorobenzyl)sulfonyl]amino)-ethyl)-1H-indol-3-yl]ethyl}sulfonyl)phenyl]-2,2-dimethylpropanoate (0.04 g, 0.05 mmol), THF (0.5 mL), MeOH (0.5 mL), and 1N 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 0.04 g of 3-[4-({2-[1-benzhydryl-5-chloro-2-(2-{[(3,4-dichlorobenzyl)sulfonyl]amino}ethyl)-1H-indol-3-yl]ethyl}sulfonyl)phenyl]-2,2-dimethylpropanoic acid as a white solid; mp 207–208° C.; MS (ESI) m/z 849.1 (M−H); HRMS: calcd for C43H41Cl3N2O6S2, 850.1472; found (ESI+), 851.1545.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101875B2
Source datasetuspto-grants-2006_09
ORD IDord-a3bd91823844484cadd47d6a32ea6be0
Source noteuspto-grants-2006_09