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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418442Generated: October 25, 2026

Allyl Isothiocyanate → 4-Allyl-3-hydroxy-5-[(5-nitrothien-2-yl)mercapto]-1,2,4-triazole

https://huagongshe.com/reaction/1418442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl IsothiocyanateHCID 5971—
Reactant2-Bromo-5-nitrothiazoleHCID 18211—
ReactantHCID 178456608HCID 178456608—
Product4-Allyl-3-hydroxy-5-[(5-nitrothien-2-yl)mercapto]-1,2,4-triazoleHCID 178456609—

Reaction Steps

The title compound was prepared in a similar manner described in Example 5 starting with allyl isothiocyanate. 4-Allyl-3-hydroxy-5-mercapto-1,2,4-triazole was reacted with 2-bromo-5-nitrothiazole as in Example 5. Crystallization from ethanol and water gave 4-allyl-3-hydroxy-5-[(5-nitrothien-2-yl)mercapto]-1,2,4-triazole as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883110
Source datasetuspto-grants-1999_03
ORD IDord-83d20bb27f9c47cc9749fe636599c5e7
Source noteuspto-grants-1999_03