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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366671Generated: November 1, 2026

Diethyl Ether → 2-(1,3-thiazol-4-ylmethyl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1366671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant2-(3-bromo-2-oxopropyl)-2,3-dihydro-1H-isoindole-1,3-dioneHCID 222037—
ReactantMethanethioamideHCID 3005587—
SolventEthanolHCID 702—
Product2-(1,3-thiazol-4-ylmethyl)-1H-isoindole-1,3(2H)-dioneHCID 21615514—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ether (7.5 mL) was added to the above solution of 2-(3-bromo-2-oxopropyl)-1H-isoindole-1,3(2H)-dione and cooled to 0° C. in an ice/NaCl salt bath. Then thioformamide (European Journal of Medicinal Chemistry, 2004, 39, 867-872.) (1.20 g) in EtOH (8 mL) was added, and the reaction was stirred overnight. The solvents were evaporated and the reaction mixture was purified by RP-HPLC to provide 2-(1,3-thiazol-4-ylmethyl)-1H-isoindole-1,3(2H)-dione as a white solid. LCMS: (M+H)+=245.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-ec3aa91637114ab394cc9cb1d14fbe43
Source noteuspto-grants-2011_02