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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354249Generated: October 31, 2026

3-Bromomethyl-5-(5-chloro-thiophen-2-yl)-isoxazole → HCID 21104891, compound

https://huagongshe.com/reaction/1354249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromomethyl-5-(5-chloro-thiophen-2-yl)-isoxazoleHCID 11150146—
ReactantHCID 67498453HCID 67498453—
SolventDimethylformamideHCID 6228—
ProductHCID 21104891HCID 21104891—

Reaction Steps

To a solution of 100 mg 2H-Tetrazole-5-carboxylic acid ethyl ester sodium salt in 1 ml DMF, 59 mg 3-Bromomethyl-5-(5-chloro-thiophen-2-yl)-isoxazole [prepared by adopting a procedure described by Ewing, William R.; Becker, Michael R.; Choi-Sledeski, Yong Mi; Pauls, Heinz W.; He, Wei; Condon, Stephen M.; Davis, Roderick S.; Hanney, Barbara A.; Spada, Alfred P.; Burns, Christopher J.; Jiang, John Z.; Li, Aiwen; Myers, Michael R.; Lau, Wan F.; Poli, Gregory B; PCT Int. Appl. (2001) 460 pp. WO 0107436 A2] were added and the mixture was stirred at room temperature for 16 h. Then the reaction mixture was concentrated under reduced pressure. The residue was taken-up in 1 ml THF and after addtion of 1 ml of a 1M NaOH solution stirred for 16 h at RT. The mixture was acidified with half concentrated hydrochloric acid to pH 3 and the precipitate collected by filtration. The product was obtained as a white solid, which was dried under reduced pressure. Yield: 49 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223780B2
Source datasetuspto-grants-2007_05
ORD IDord-114c6522764b4ac597390a0a0c117194
Source noteuspto-grants-2007_05