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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066742Generated: November 1, 2026

Sodium Carbonate → 6-[2-(4-Benzo[d]isothiazol-3-yl-piperazin-1-yl)-ethyl]-3H-benzooxazol-2-one

https://huagongshe.com/reaction/1066742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-(1-Piperazinyl)-1,2-benzisothiazoleHCID 2772144—
Reactant6-BromoethylbenzoxazoloneHCID 13306087—
SolventMethyl Isobutyl KetoneHCID 7909—
Product6-[2-(4-Benzo[d]isothiazol-3-yl-piperazin-1-yl)-ethyl]-3H-benzooxazol-2-oneHCID 10809803—

Reaction Steps

To a 125 ml round-bottomed flask equipped with condenser were added 4.82 grams (0.022 mol) of N-(3-benzoisothiazolyl)piperazine (prepared according to the procedure given in U.S. Pat. No. 4,411,901), 5.32 grams (0.022 mol) of 6-(2-bromo)ethylbenzoxazolone, 2.33 grams (0.022 mol) of sodium carbonate, and 50 ml of methyl isobutyl ketone. The mixture was refluxed for 18 hours. The reaction was cooled and partitioned between ethyl acetate and water. The ethyl acetate layer was isolated, washed with water and saturated aqueous sodium chloride solution dried over sodium sulfate, and evaporated to an oil. The oil was chromatographed on silica gel using ethyl acetate as eluent, and the product fractions collected and triturated with methylene chloride/isopropyl ether to give a white solid, 1 m.p. 185°-187° C. NMR (CDCl3): 1.7 (bs, 1 H), 2.8 (m, 8H), 3.6 (m, 4H), 6.9-8.0 (m, 7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245766B1
Source datasetuspto-grants-2001_06
ORD IDord-d6e1773fe4724956bd54ee63b461a168
Source noteuspto-grants-2001_06