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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739382Generated: November 2, 2026

HCID 21840896, compound → HCID 54375973, compound

https://huagongshe.com/reaction/1739382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21840896HCID 21840896—
ReactantHCID 72590775HCID 72590775—
SolventMethanolHCID 887—
ProductHCID 54375973HCID 5437597355.4%

Reaction Steps

To 0.23 g (1 mmol) of 5-(2-formyl-α-methoxybenzyl)-3-methylthiazole in 2 ml of methanol was added 0.22 g (1.1 mmol) of 4'-(trifluoromethyl)acetophenone hydrazone and stirred at room temperature for 3 hours. After completion of the reaction, methanol was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate/n-hexane) to give 5-[α-methoxy-2-{4-(4-trifluoromethylphenyl)-2,3-diaza-1,3-pentadienyl}benzyl]-3-methylthiazole (0.23 g, 55.4%) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965740
Source datasetuspto-grants-1999_10
ORD IDord-ff80e5a3dd82458f95ed380847bfde24
Source noteuspto-grants-1999_10