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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220148Generated: October 29, 2026

Sodium Hydroxide → HCID 23134795, compound

https://huagongshe.com/reaction/2220148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 23134769HCID 23134769—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23134795HCID 23134795—

Reaction Steps

To a solution of ethyl 3-[N-[[4-[2-(3-triphenylmethyl-3H-tetrazol-5-yl)phenyl]phenyl]methyl]-N-pentanoylamino]benzoate (11.50 g) synthesized in Example 1a in dioxane (100 ml) was added 1N-aqueous sodium hydroxide solution (19 ml), and the mixture was stirred at room temperature for 5 days. The reaction mixture was concentrated, ethyl acetate and saturated aqueous potassium bisulfate solution were added to carry out partitioning and extraction. The extracted organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, filtrated and concentrated to give a crude product of 3-[N-[[4-[2-(3-triphenylmethyl-3H-tetrazol-5-yl)phenyl]phenyl]methyl]-N-pentanoylamino]benzoic acid. To a solution of the obtained crude product in DMA (90 ml) were added potassium carbonate (4.86 g) and a solution of 4-chloromethyl-5-methyl-1,3-dioxolen-2-one (3.92 g) in DMA (5 ml), and the mixture was stirred at room temperature for 24 hrs. The reaction mixture was poured into ethyl acetate-water to carry out partitioning and extraction. The extracted organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, filtrated and concentrated, and the residue was purified by silica gel column chromatography (hexane-ethyl acetate:1-1 v/v) to give (5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl3-[N-[[4-[2-(3-triphenylmethyl-3H-tetrazol-5-yl)phenyl]phenyl]methyl]-N-pentanoylamino]benzoate (11.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417052B2
Source datasetuspto-grants-2008_08
ORD IDord-ec9a6c588a6f49048c00cc6b555b88cd
Source noteuspto-grants-2008_08