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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403414Generated: November 1, 2026

Benzothiazole → HCID 70664862, compound

https://huagongshe.com/reaction/1403414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantMethyl 2-chloro-3-(isopropyl(methyl)amino)quinoxaline-6-carboxylateHCID 86667203—
ReactantHCID 178476685HCID 178476685—
CatalystHCID 178418397HCID 178418397—
ProductHCID 70664862HCID 706648629.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

Into a 10-mL sealed was placed methyl 2-chloro-3-[methyl(propan-2-yl)amino]quinoxaline-6-carboxylate (400 mg, 1.36 mmol), 1,3-benzothiazole (368 mg, 2.72 mmol), Pd(PPh3)4 (80 mg, 0.06 mmol) and AcOK (272 mg, 2.72 mmol) under nitrogen atmosphere. After stirring 4 h at 150° C., the reaction mixture was purified by silica gel column chromatography eluting with 10% ethyl acetate in petroleum ether to afford methyl 2-(1,3-benzothiazol-2-yl)-3-[methyl(propan-2-yl)amino]quinoxaline-6-carboxylate as a light yellow solid (50 mg, 9.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-7a29b978fa904d7cae00e6fc5d9ba8f9
Source noteuspto-grants-2014_12