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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477595Generated: October 25, 2026

Water → 2-[3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazolon-5-yl]4,5,6,7-tetrahydro-2H-isoindole-1,3-dione

https://huagongshe.com/reaction/477595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
Reactant5-amino-3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazoloneHCID 14014245—
SolventAcetic AcidHCID 176—
Product2-[3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazolon-5-yl]4,5,6,7-tetrahydro-2H-isoindole-1,3-dioneHCID 1401424619.1%

Reaction Steps

5-Amino-3-ethoxycarbonylmethyl-6-fluoro-2(3H)benzothiazolone (140 mg) and 3,4,5,6-tetrahydrophthalic anhydride (90 mg) were suspended in acetic acid (3 ml), and the resultant suspension was heated under reflux for 5 hours. After being allowed to cool, water was added thereto, and the resultant mixture was extracted with ethyl acetate. The extract ws washed with water and sodium bicarbonte solution, dried and concentrated. The residue was purified by silica gel thin layer chromatography with a mixture of ethyl acetate and hexane (1:2) to give 2-[3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazolon-5-yl]4,5,6,7-tetrahydro-2H-isoindole-1,3-dione (40 mg). m.p., 155.5°-156.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888428
Source datasetuspto-grants-1989_12
ORD IDord-6315777bab0346709ccb5beb232dceb4
Source noteuspto-grants-1989_12