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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-(3-bromo-2-oxopropyl)-2,3-dihydro-1H-isoindole-1,3-dione | HCID 222037 | — |
| Reactant | Methanethioamide | HCID 3005587 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(1,3-thiazol-4-ylmethyl)-1H-isoindole-1,3(2H)-dione | HCID 21615514 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893056B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-ec3aa91637114ab394cc9cb1d14fbe43 |
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| Source note | uspto-grants-2011_02 |
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