Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642680Generated: October 30, 2026

Azetidine → HCID 58900220, compound

https://huagongshe.com/reaction/642680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzetidineHCID 10422—
ReactantHCID 86613188HCID 86613188—
SolventDichloromethaneHCID 6344—
ProductHCID 58900220HCID 58900220—

Reaction Steps

To a solution of 6-fluoro-9-naphthalen-1-ylmethyl-4,9-dihydro-pyrano[3,4-b]indole-1,3-dione (1.0 mmole) in CH2Cl2 (3 ml) was added azetidine(5 mmole) and stirring was continued at 22° C. until completion of the reaction. The mixture was evaporated and the residue partitioned between aqueous HCl and AcOEt. The organic layer was dried, evaporated and the residue triturated with diethylether to give 3-(2-azetidin-1-yl-2-oxo-ethyl)-5-fluoro-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid as a white solid. MS: 417.4 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696240B2
Source datasetuspto-grants-2010_04
ORD IDord-19e48edaafed43eabf38ec6ee9a4c17d
Source noteuspto-grants-2010_04