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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655894Generated: November 1, 2026

Benzenethiol, 2-amino-, hydrochloride (1:1) → Ethyl 2-[4-(benzothiazol-2-yl)methyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl]acetate

https://huagongshe.com/reaction/1655894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenethiol, 2-amino-, hydrochloride (1:1)HCID 76794—
ReactantEthyl 2-(4-cyanomethyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl)acetateHCID 10062806—
SolventWaterHCID 962—
ProductEthyl 2-[4-(benzothiazol-2-yl)methyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl]acetateHCID 997820468.7%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 208 mg of ethyl 2-(4-cyanomethyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl)acetate and 116 mg of 2-aminothiophenol hydrochloride was heated at 180° C. for 15 minutes to fuse them. After the mixture had been cooled, water was added, and then extracted with ethyl acetate. After the drying of the organic layer over anhydrous magnesium sulfate, the solvent was distilled off. The resulting oily matter was purified by silica gel chromatography to give 196 mg of the title compound. The structural formula and physical data of this compound are shown in Table 15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252571
Source datasetuspto-grants-1993_10
ORD IDord-c897ccbf25c14139924b6ecfb0f78c98
Source noteuspto-grants-1993_10