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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837938Generated: November 4, 2026

Benzothiazole → HCID 53757231, compound

https://huagongshe.com/reaction/1837938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 54554919HCID 54554919—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53757231HCID 53757231—

Reaction Steps

To a stirred solution of benzthiazole (165 mg, 1.22 mmol) in anhydrous tetrahydrofuran (5 mL) at −78° C. was added a solution of n-butyllithium in hexanes (0.52 mL of a 2.5 M solution). After 5 minutes, a solution of zinc chloride in tetrahydrofuran (2.6 mL of a 0.50 M solution) was added and the reaction mixture was allowed to warm to ambient temperature. To the resulting solution was added 9-(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-yl)-3-(trifluoromethanesulfonyloxy)-non-2-enoic acid tert-butyl ester 29-6 (400 mg, 0.81 mmol) and palladium(tetrakis)-triphenylphosphine (94 mg, 0.081 mmol) and the mixture was stirred at ambient temperature for 1 hour. The reaction mixture was then poured into saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried with anhydrous magnesium sulfate, filtered, and concentrated at reduced pressure. The resulting oil was purified by flash column chromatography over silica gel with 4:1 ethyl acetate/hexanes to give 29-7c as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784190B2
Source datasetuspto-grants-2004_08
ORD IDord-73d5c3c2debe4b94998f1f4b36949b5f
Source noteuspto-grants-2004_08