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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241961Generated: October 26, 2026

Benzothiazolium, 3-methyl-2-(methylthio)-, 4-methylbenzenesulfonate (1:1) → 2-(3-acetylphenylimino)-5-(3-methyl-3H-benzothiazol-2-ylidene)-3-pyridin-3-ylmethylthiazolidin-4-one

https://huagongshe.com/reaction/1241961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazolium, 3-methyl-2-(methylthio)-, 4-methylbenzenesulfonate (1:1)HCID 41464—
Reactant2-(3-Acetylphenylimino)-3-pyridin-3-ylmethylthiazolidin-4-oneHCID 21937348—
Product2-(3-acetylphenylimino)-5-(3-methyl-3H-benzothiazol-2-ylidene)-3-pyridin-3-ylmethylthiazolidin-4-oneHCID 73855000—

Reaction Steps

The title compound was prepared from intermediate 2-(3-acetylphenylimino)-3-pyridin-3-ylmethylthiazolidin-4-one and 3-methyl-2-(methylthio)benzothiazol-3-ium p-toluenesulfonate as described in Example 45. 1H-NMR (CDCl3): δ 8.87 (1H, d), 8.56 (1H, dd), 7.93 (1H, m), 7.74 (1H, m), 7.60 (1H, m), 7.53 (1H, d), 7.46 (1H, m), 7.27–7.38 (2H, m), 7.17–7.23 (2H, m), 7.05 (1H, d), 5.18 (2H, s), 3.74 (3H, s), 2.62 (3H, s); MS(ESI): 473 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115640B2
Source datasetuspto-grants-2006_10
ORD IDord-219ad8cb787742638288eb08238d0f43
Source noteuspto-grants-2006_10