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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13408Generated: October 29, 2026

Acetic Anhydride → HCID 23145654, compound

https://huagongshe.com/reaction/13408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 23145247HCID 23145247—
SolventChloroformHCID 6212—
ProductHCID 23145654HCID 23145654—

Reaction Steps

0.003 ml of acetic anhydride was added to a chloroform (1 ml) solution of 5.8 mg of 5′-((2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazol-5-yl)oxy)-2H-1,2′-bipyridin-2-one enantiomer B obtained in Example 554, and the reaction liquid was stirred at room temperature for 30 minutes. The reaction solvent was evaporated away, and the resulting residue was purified through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=10/1) to obtain one chiral form of the entitled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-096b9e7546e4466ea8fd0595d285fae1
Source noteuspto-grants-2010_06